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Sample records for capacity mercury adsorption

  1. High capacity mercury adsorption on freshly ozone-treated carbon surfaces

    OpenAIRE

    Manchester, Shawn; Wang, Xuelei; Kulaots, Indrek; Gao, Yuming; Hurt, Robert H.

    2008-01-01

    A set of carbon materials was treated by a choice of common oxidizers to investigate the mercury capture capacities at varying temperature conditions. It was found that ozone treatment dramatically increases the mercury capture capacity of carbon surfaces by factors up to 134, but the activity is easily destroyed by exposure to the atmosphere, to water vapor, or by mild heating. Freshly ozone-treated carbon surfaces are shown to oxidize iodide to iodine in solution and this ability fades with...

  2. Removal of mercury by adsorption: a review.

    Science.gov (United States)

    Yu, Jin-Gang; Yue, Bao-Yu; Wu, Xiong-Wei; Liu, Qi; Jiao, Fei-Peng; Jiang, Xin-Yu; Chen, Xiao-Qing

    2016-03-01

    Due to natural and production activities, mercury contamination has become one of the major environmental problems over the world. Mercury contamination is a serious threat to human health. Among the existing technologies available for mercury pollution control, the adsorption process can get excellent separation effects and has been further studied. This review is attempted to cover a wide range of adsorbents that were developed for the removal of mercury from the year 2011. Various adsorbents, including the latest adsorbents, are presented along with highlighting and discussing the key advancements on their preparation, modification technologies, and strategies. By comparing their adsorption capacities, it is evident from the literature survey that some adsorbents have shown excellent potential for the removal of mercury. However, there is still a need to develop novel, efficient adsorbents with low cost, high stability, and easy production and manufacture for practical utility. PMID:26620868

  3. Preparation of hybrid organic-inorganic mesoporous silicas applied to mercury removal from aqueous media: Influence of the synthesis route on adsorption capacity and efficiency.

    Science.gov (United States)

    Pérez-Quintanilla, Damián; Sánchez, Alfredo; Sierra, Isabel

    2016-06-15

    New hybrid organic-inorganic mesoporous silicas were prepared by employing three different synthesis routes and mercury adsorption studies were done in aqueous media using the batch technique. The organic ligands employed for the functionalization were derivatives of 2-mercaptopyrimidine or 2-mercaptothiazoline, and the synthesis pathways used were post-synthesis, post-synthesis with surface ion-imprinting and co-condensation with ion-imprinting. The incorporation of functional groups and the presence of ordered mesopores in the organosilicas was confirmed by XRD, TEM and SEM, nitrogen adsorption-desorption isotherms, (13)C MAS-NMR, (29)Si MAS-NMR, elemental and thermogravimetric analysis. The highest adsorption capacity and selectivity observed was for the material functionalized with 2-mercaptothiazoline ligand by means the co-condensation with ion-imprinting route (1.03 mmol g(-1) at pH 6). The prepared material could be potential sorbent for the extraction of this heavy metal from environmental and drinking waters.

  4. Preparation of hybrid organic-inorganic mesoporous silicas applied to mercury removal from aqueous media: Influence of the synthesis route on adsorption capacity and efficiency.

    Science.gov (United States)

    Pérez-Quintanilla, Damián; Sánchez, Alfredo; Sierra, Isabel

    2016-06-15

    New hybrid organic-inorganic mesoporous silicas were prepared by employing three different synthesis routes and mercury adsorption studies were done in aqueous media using the batch technique. The organic ligands employed for the functionalization were derivatives of 2-mercaptopyrimidine or 2-mercaptothiazoline, and the synthesis pathways used were post-synthesis, post-synthesis with surface ion-imprinting and co-condensation with ion-imprinting. The incorporation of functional groups and the presence of ordered mesopores in the organosilicas was confirmed by XRD, TEM and SEM, nitrogen adsorption-desorption isotherms, (13)C MAS-NMR, (29)Si MAS-NMR, elemental and thermogravimetric analysis. The highest adsorption capacity and selectivity observed was for the material functionalized with 2-mercaptothiazoline ligand by means the co-condensation with ion-imprinting route (1.03 mmol g(-1) at pH 6). The prepared material could be potential sorbent for the extraction of this heavy metal from environmental and drinking waters. PMID:27023632

  5. Mercury adsorption properties of sulfur-impregnated adsorbents

    Science.gov (United States)

    Hsi, N.-C.; Rood, M.J.; Rostam-Abadi, M.; Chen, S.; Chang, R.

    2002-01-01

    Carbonaceous and noncarbonaceous adsorbents were impregnated with elemental sulfur to evaluate the chemical and physical properties of the adsorbents and their equilibrium mercury adsorption capacities. Simulated coal combustion flue gas conditions were used to determine the equilibrium adsorption capacities for Hg0 and HgCl2 gases to better understand how to remove mercury from gas streams generated by coal-fired utility power plants. Sulfur was deposited onto the adsorbents by monolayer surface deposition or volume pore filling. Sulfur impregnation increased the total sulfur content and decreased the total and micropore surface areas and pore volumes for all of the adsorbents tested. Adsorbents with sufficient amounts of active adsorption sites and sufficient microporous structure had mercury adsorption capacities up to 4,509 ??g Hg/g adsorbent. Elemental sulfur, organic sulfur, and sulfate were formed on the adsorbents during sulfur impregnation. Correlations were established with R2>0.92 between the equilibrium Hg0/HgCl2 adsorption capacities and the mass concentrations of elemental and organic sulfur. This result indicates that elemental and organic sulfur are important active adsorption sites for Hg0 and HgCl2.

  6. Enhanced mercury ion adsorption by amine-modified activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Zhu Jianzhong [Center of Environmental Sciences, Lincoln University of Missouri, Jefferson City, MO 65102 (United States); Yang, John, E-mail: yangj@lincolnu.edu [Center of Environmental Sciences, Lincoln University of Missouri, Jefferson City, MO 65102 (United States); Deng Baolin [Department of Civil and Environmental Engineering, University of Missouri, Columbia, MO 65211 (United States)

    2009-07-30

    Mercury (Hg) is one of the most toxic metals found in water and sediments. In an effort to develop an effective adsorbent for aqueous Hg removal, activated carbon (AC) was modified with an amino-terminated organosilicon (3-aminopropyltriethoxysilane, APTES). Surface properties of the APTES-modified AC (MAC) were characterized by the scanning electron microscopy in conjunction with the energy-dispersive spectroscopy (SEM-EDS), the Fourier transform infrared spectroscopy (FT-IR), and potentiometry. The impacts of solvent, APTES concentration, reactive time and temperature on the surface modification were evaluated. The aqueous Hg adsorptive kinetics and capacity were also determined. Results demonstrated that the strong Hg-binding amine ligands were effectively introduced onto the AC surfaces through the silanol reaction between carbon surface functional groups (-COOH, -COH) and APTES molecules. The modification lowered the pH at the point of zero charge (pH{sub pzc}) to 4.54 from 9.6, favoring cation adsorption. MAC presented a faster rate of the Hg (II) adsorption and more than double adsorptive capacity as compared with AC.

  7. Vapor-phase elemental mercury adsorption by residual carbon separated from fly ash

    Institute of Scientific and Technical Information of China (English)

    WANG Li-gang; CHEN Chang-he; Kruse H.Kolker

    2005-01-01

    The adsorption capacity for vapor-phase elemental mercury(Hg0 ) of residual carbon separated from fly ash was studied in an attempt for the control of elemental mercury emissions from combustion processes. At Iow mercury concentrations ( < 200 μg/m3),unburned carbon had higher adsorption capacity than commercial activated carbon. The adsorbality of unburned carbon was also found to be source dependent. Isotherms of FS carbon(separated from fly ash of a power plant of Shishi in Fujian Province) were similar to those classified as type Ⅱ. Isotherms of XJ carbon (separated from fly ash of a power plant of Jingcheng in Shanxi Province) were more like those classified as type Ⅲ. Due to the relatively Iow production costs, these residual carbons would likely be considerably more costeffective for the full-scale removal of mercury from combustion flue gases than other technology.

  8. Effect of oxidation treatment on the adsorption and the stability of mercury on activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Hu, C.X.; Zhou, J.S.; Luo, Z.Y.; He, S.; Wang, G.K.; Cen, K.F. [Zhejiang University, Hangzhou (China)

    2006-07-01

    Oxidation treatment on the adsorption and the stability of Hg on activated carbon (AC) was investigated. Both MnO{sub 2}-AC and FeCl{sub 3}-AC were produced during oxidation treatment. The measurement of modified AC's mercury adsorption capacity was conducted in a simulated coal-fired flue gas by adsorbing test apparatus. TCLP and column leaching methods were used to test the stability of mercury adsorbed on ACs. The results indicate that the oxidation treatment changed the pore structure of the AC and modified the carbon surface by creating chemical components such as MnO{sub 4}{sup -}, Mn{sup 4+}, NO{sub 3}{sup -}, Fe{sup 3+} Cl{sup -}, etc. The Hg sorption capacity on MnO{sub 2}-AC or FeCl3-AC was about three times higher than that of untreated carbon. In addition, the mercury control cost of each of the formers was about the half cost of the untreated carbon. The stability of Hg absorption was studied. It was found that mercury adsorbed on the oxidation treated AC was not better than that of untreated carbon. It could be concluded that the insoluble form of Hg is very important to the stability of mercury adsorbed on AC. This study suggests that the FeCl3-AC is the best absorbent for Hg with high adsorption capacity, better Hg adsorption stability in leaching environment, and lower cost among the three ACs tested.

  9. Effect of oxidation treatment on the adsorption and the stability of mercury on activated carbon

    Institute of Scientific and Technical Information of China (English)

    HU Chang-xing; ZHOU Jin-song; LUO Zhong-yang; HE Sheng; WANG Guang-kai; CEN Ke-fa

    2006-01-01

    Oxidation treatment on the adsorption and the stability of Hg on activated carbon (AC) was inrestigated. Both MnO2-AC and FeCl3-AC were produced during oxidation treatment. The measurement of modified AC's mercury adsorption capacity was conducted in a simulated coal-fired flue gas by adsorbing test apparatus. TCLP and column leaching methods were used to test the stability of mercury adsorbed on ACs. The results indicate that the oxidation treatment changed the pore structure of the AC and modified the carbon surface by creating chemical components such as MnO4-, Mn4+, O, NO3-, Fe3+, Cl-, etc. The Hg sorption capacity on MnO2-AC or FeCl3-AC was about three times higher than that of untreated carbon. In addition, the mercury control cost of each of the formers was about the half cost of the untreated carbon. The stability of Hg absorption was studied, it found that mercury adsorbed on the oxidation treated AC was not better than that of untreated carbon. It could concluded that the insoluble form of Hg is very important to the stability of mercury adsorbed on AC. This study suggests that the FeCl3-AC is the best absorbent for Hg with high adsorption capacity, better Hg adsorption stability in leaching environment, and lower cost among the three ACs tested.

  10. Adsorption of mercury (II from liquid solutions using modified activated carbons

    Directory of Open Access Journals (Sweden)

    Hugo Soé Silva

    2010-06-01

    Full Text Available Mercury is one of the most toxic metals present in the environment. Adsorption has been proposed among the technologies for mercury abatement. Activated carbons are universal adsorbents which have been found to be a very effective alternative for mercury removal from water. The effectiveness with which a contaminant is adsorbed by the solid surface depends, among other factors, on the charge of the chemical species in which the contaminant is in solution and on the net charge of the adsorbent surface which depend on the pH of the adsorption system. In this work, activated carbon from carbonized eucalyptus wood was used as adsorbent. Two sulphurization treatments by impregnation with sulphuric acid and with carbon disulphide, have been carried out to improve the adsorption capacity for mercury entrapment. Batch adsorption tests at different temperatures and pH of the solution were carried out. The influence of the textural properties, surface chemistry and operation conditions on the adsorption capacity, is discussed.

  11. Adsorption of azithromycin dehydrate at stationary mercury and solid electrode

    OpenAIRE

    Karbainov, Yu. A.; Puchkovskaya, E. S.; Karbainova, S. N.

    2007-01-01

    Adsorptive component in oxidation and renewal processes at different types of electrodes for antibiotic-macrolide azithromycin dihydrate has been studied. Adsorption parameters for azithromycin oxidation processes at glass-carbon electrode and for renewal processes at mercury-film electrode were calculated

  12. Evidence of the direct adsorption of mercury in human hair during occupational exposure to mercury vapour.

    Science.gov (United States)

    Queipo Abad, Silvia; Rodríguez-González, Pablo; García Alonso, J Ignacio

    2016-07-01

    We have found clear evidence of direct adsorption of mercury in human hair after the occupational exposure to mercury vapour. We have performed both longitudinal analysis of human hair by laser ablation ICP-MS and speciation analysis by gas chromatography ICP-MS in single hair strands of 5 individuals which were occupationally exposed to high levels of mercury vapour and showed acute mercury poisoning symptoms. Hair samples, between 3.5 and 11cm long depending on the individual, were taken ca. three months after exposure. Single point laser ablation samples of 50μm diameter were taken at 1mm intervals starting from the root of the hairs. Sulfur-34 was used as internal standard. The ratio (202)Hg/(34)S showed a distinct pattern of mercury concentration with much lower levels of mercury near the root of the hair and high levels of mercury near the end of the hair. In all cases a big jump in the concentration of mercury in hair occurred at a given distance from the root, between 32 and 42mm depending on the individual, with a high and almost constant concentration of mercury for longer distances to the root. When we took into account the rate of hair growth in humans, 9-15mm/month, the jump in mercury concentration agreed approximately with the dates when the contamination occurred with the new growing hair showing much lower mercury concentration. In some cases the concentration of mercury at the tip of the hair was ca. 1000 times higher than that near the root. Additionally, speciation studies confirmed that mercury in all hair samples was present as inorganic mercury. The only explanation for these results was the direct adsorption of mercury vapour in hair at the time of exposure. PMID:27259347

  13. Mechanisms of CPB Modified Zeolite on Mercury Adsorption in Simulated Wastewater.

    Science.gov (United States)

    Liu, Jiang; Huang, Hui; Huang, Rong; Zhang, Jinzhong; Hao, Shuoshuo; Shen, Yuanyuan; Chen, Hong

    2016-06-01

    A systematic study was carried out to analyze the effects of mercury(II) adsorption by surface modified zeolite (SMZ) and adsorption mechanism. Cetylpyridinium bromide (CPB) was used to prepare SMZ. The characterization methods by means of powder X-ray diffraction (XRD), Fourier transform infrared (FT-IR), scanning electron microscope (SEM) showed that both the surface and internal zeolite were covered with CPB molecules, but the main binding sites were surface. Results showed that the organic carbon and cation exchange capacity of the SMZ were 7.76 times and 4.22 times higher than those of natural zeolite (NZ), respectively. Zeta potentials before and after modification were measured at -7.80 mV and -30.27 mV, respectively. Moreover, the saturation adsorptive capacity of SMZ was 16.35 times higher than NZ in mercury-containing wastewater. The possible mechanisms of mercury elimination were surface adsorption, hydrophobic interaction, ion exchange, electricity neutralization. The adsorption process was affected little by competitive ions.

  14. Development of coconut pith chars towards high elemental mercury adsorption performance - Effect of pyrolysis temperatures.

    Science.gov (United States)

    Johari, Khairiraihanna; Saman, Norasikin; Song, Shiow Tien; Cheu, Siew Chin; Kong, Helen; Mat, Hanapi

    2016-08-01

    In this study, chars from coconut pith (CP) were prepared aiming for superior adsorption towards elemental mercury (Hg(o)). The yield, proximate analysis, textural characteristics, surface functional groups and elemental composition analyses of the chars produced at pyrolysis temperature of 300 °C, 500 °C, 700 °C and 900 °C were compared. The surface area, pore volume, ash and carbon content of chars increased, while the yield and moisture content decreased with increasing pyrolysis temperatures. The changing of physical and chemical properties of the chars produced at variety pyrolysis temperature was much effect on the Hg(o) adsorption performance and definitely provides important information on the Hg(o) adsorption mechanism. The highest Hg(o) adsorption capacity was observed for CP900 (6067.49 μg/g), followed by CP700 (2395.98 μg/g), CP500 (289.76 μg/g), CP300 (1.68 μg/g), and CP (0.73 μg/g). The equilibrium data were well described by the Freundlich adsorption isotherm model. The pseudo-second order best described the kinetic data of the Hg(o) adsorption onto CP and CP300. For chars produced at higher pyrolysis temperature, however, the pseudo-zero order and pseudo-second order fitted well for the adsorption and breakthrough regions, respectively. The Hg(o) adsorption capacity of chars obtained from high pyrolysis temperature of CP significantly outperformed the commercial activated carbon (Darco KB-B) as well as superior to chars reported in the literature indicating the CP can be used as a precursor for preparation of chars as elemental mercury adsorbents. PMID:27160635

  15. Development of coconut pith chars towards high elemental mercury adsorption performance - Effect of pyrolysis temperatures.

    Science.gov (United States)

    Johari, Khairiraihanna; Saman, Norasikin; Song, Shiow Tien; Cheu, Siew Chin; Kong, Helen; Mat, Hanapi

    2016-08-01

    In this study, chars from coconut pith (CP) were prepared aiming for superior adsorption towards elemental mercury (Hg(o)). The yield, proximate analysis, textural characteristics, surface functional groups and elemental composition analyses of the chars produced at pyrolysis temperature of 300 °C, 500 °C, 700 °C and 900 °C were compared. The surface area, pore volume, ash and carbon content of chars increased, while the yield and moisture content decreased with increasing pyrolysis temperatures. The changing of physical and chemical properties of the chars produced at variety pyrolysis temperature was much effect on the Hg(o) adsorption performance and definitely provides important information on the Hg(o) adsorption mechanism. The highest Hg(o) adsorption capacity was observed for CP900 (6067.49 μg/g), followed by CP700 (2395.98 μg/g), CP500 (289.76 μg/g), CP300 (1.68 μg/g), and CP (0.73 μg/g). The equilibrium data were well described by the Freundlich adsorption isotherm model. The pseudo-second order best described the kinetic data of the Hg(o) adsorption onto CP and CP300. For chars produced at higher pyrolysis temperature, however, the pseudo-zero order and pseudo-second order fitted well for the adsorption and breakthrough regions, respectively. The Hg(o) adsorption capacity of chars obtained from high pyrolysis temperature of CP significantly outperformed the commercial activated carbon (Darco KB-B) as well as superior to chars reported in the literature indicating the CP can be used as a precursor for preparation of chars as elemental mercury adsorbents.

  16. Adsorption of mercury in coal-fired power plants gypsum slurry on TiO2/chitosan composite material

    Science.gov (United States)

    Gao, P.; Gao, B. B.; Gao, J. Q.; Zhang, K.; Chen, Y. J.; Yang, Y. P.; Chen, H. W.

    2016-07-01

    In this study, a simple method was used to prepare a chitosan adsorbent to mix with KI and TiO2. Gravimetric analysis (TG), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) were used to characterize the samples before and after adsorption of Hg2+. A mercury adsorption experiment was also conducted in the gypsum slurry. The results show that using hydrobromic acid as a solvent of adsorbent resulted in a better adsorption effect than using acetic acid alone. Also, the sample (CS-KI/TiO2-HBr) had a maximum mercury adsorption capacity when the pH=5 and the t=50°C. The characterization experiments showed that the thermal stability of composite materials declined and the TiO2 uniformly dispersed in the surface of the samples with a lamellar structure, generating a lot of cracks and recesses that increased the reactive sites. Furthermore, when the TiO2 reacted with CS, it resulted in Ti-C, Ti-O and Ti-N bonds. The Br- can prevent the growth of TiO2 crystal grains and strengthen the ability of I- to remove mercury. The adsorption isotherm and kinetic results indicated that the adsorption behaviour of CS-KI/TiO2-HBr as it removes Hg2+ is an inhomogeneous multilayer adsorption process. The surface adsorption and intraparticle diffusion effects are both important in the Hg2+ adsorption process.

  17. Thorough removal of inorganic and organic mercury from aqueous solutions by adsorption on Lemna minor powder

    Energy Technology Data Exchange (ETDEWEB)

    Li Shunxing, E-mail: lishunxing@fjzs.edu.cn [Department of Chemistry, Zhangzhou Normal University, Zhangzhou 363000 (China); Fujian Province University Key Laboratory of Analytical Science, Zhangzhou Normal University, Zhangzhou (China); Zheng Fengying; Huang Yang [Department of Chemistry, Zhangzhou Normal University, Zhangzhou 363000 (China); Fujian Province University Key Laboratory of Analytical Science, Zhangzhou Normal University, Zhangzhou (China); Ni Jiancong [Department of Chemistry, Zhangzhou Normal University, Zhangzhou 363000 (China)

    2011-02-15

    The adsorption ability of duckweed (Lemna minor) powders for removing inorganic and organic mercury (methyl and ethyl mercury) has been studied using cold vapour atomic absorption spectrometry. The optimal adsorption conditions were: (a) the pH value of the solution 7.0 for inorganic and ethyl mercury, 9.0 for methyl mercury, and (b) equilibrium adsorption time 10, 20, and 40 min for inorganic mercury, methyl mercury, and ethyl mercury, respectively. After adsorption by L. minor powder for 40 min, when the initial concentrations of inorganic and organic mercury were under 12.0 {mu}g L{sup -1} and 50.0 {mu}g L{sup -1}, respectively, the residual concentrations of mercury could meet the criterion of drinking water (1.0 {mu}g L{sup -1}) and the permitted discharge limit of wastewater (10.0 {mu}g L{sup -1}) set by China and USEPA, respectively. Thorough removal of both inorganic and organic mercury from aqueous solutions was reported for the first time. The significant adsorption sites were C-O-P and phosphate groups by the surface electrostatic interactions with aqueous inorganic and organic mercury cations, and then the selective adsorption was resulted from the strong chelating interaction between amine groups and mercury on the surface of L. minor cells.

  18. Adsorption and Desorption of Mercury(II) in Three Forest Soils in Shandong Province, China

    Institute of Scientific and Technical Information of China (English)

    XUE Tong; WANG Ren-Qing; ZHANG Meng-Meng; DAI Jiu-Lan

    2013-01-01

    As one of the most toxic heavy metals with persistence,bioaccumulation,and toxicity in environment,mercury and its environmental problems have caused a global concern.To fully understand the behavior and fate of mercury (Hg)(II) in forest soils,a series of batch experiments were conducted to determine the adsorption and desorption characteristics of Hg(II) by three dark brown forest soils from Mount Taishan,Laoshan Mountain,and Fanggan Village in Shandong Province,China.The adsorption solution was prepared using 0.1 mol L-1 NaNO3 as background electrolyte,with Hg(II) at rising concentration gradients of 0.0,2.0,4.0,6.0,8.0,and 10.0 mg L-1.Fourier transform infrared (FTIR) spectroscopy was adopted to characterize the soil samples and soil-Hg complexes.It was found that Hg(II) adsorption isotherms could be well fitted with both Langmuir and Freundlich equations.The soil from Mount Taishan had the largest potential Hg(II) adsorption capacity,though with less adsorptive intensity.The percentages of Hg(II) desorbed from all soil samples were less than 0.6%,which suggested that all the soils studied had a high binding strength for Hg(II).The soil from Mount Taishan had a higher Hg(II) desorption capacity than the other soils,which indicated that the Hg(II) deposited on the topsoil of Mount Taishan from atmosphere may easily discharge to surface water through runoff.Results of the FTIR spectroscopy showed that the three soils contained the same functional groups.The relative absorbencies of soil-Hg complexes changed significantly compared with those of the soil samples and the adsorption of Hg(II) mainly acted on the O-H,C-O,and C=O groups of the soils.

  19. Influence of the pore structure and surface chemical properties of activated carbon on the adsorption of mercury from aqueous solutions

    International Nuclear Information System (INIS)

    Highlights: • Activated carbons with different pore structure and surface chemical properties were prepared by modification process. • HgCl2 as a pollution target to evaluate the adsorption performance. • Influence of pore structure and surface chemical properties of activated carbon on adsorption of mercury was investigated. -- Abstract: Reactivation and chemical modification were used to obtain modified activated carbons with different pore structure and surface chemical properties. The samples were characterized by nitrogen absorption–desorption, Fourier transform infrared spectroscopy and the Bothem method. Using mercury chloride as the target pollutant, the Hg2+ adsorption ability of samples was investigated. The results show that the Hg2+ adsorption capacity of samples increased significantly with increases in micropores and acidic functional groups and that the adsorption process was exothermic. Different models and thermodynamic parameters were evaluated to establish the mechanisms. It was concluded that the adsorption occurred through a monolayer mechanism by a two-speed process involving both rapid adsorption and slow adsorption. The adsorption rate was determined by chemical reaction

  20. Adsorption of mercury ions by mercapto-functionalized amorphous silica

    Energy Technology Data Exchange (ETDEWEB)

    Perez-Quintanilla, Damian; Hierro, Isabel del; Fajardo, Mariano; Sierra, Isabel [Universidad Rey Juan Carlos, Departamento de Tecnologia Quimica y Ambiental, E.S.C.E.T, Mostoles, Madrid (Spain); Carrillo-Hermosilla, Fernando [Universidad de Castilla-La Mancha, Departamento de Quimica Inorganica, Organica y Bioquimica, Facultad de Quimicas, Ciudad Real (Spain)

    2006-02-01

    Amorphous silicas have been functionalized by two different methods. In the heterogeneous route the silylating agent, 3-chloropropyltriethoxysilane, was initially immobilized onto the silica surface to give the chlorinated silica Cl-Sil. In a second reaction, multifunctionalized N,S donor compounds were incorporated to obtain the functionalized silicas, which are denoted as L-Sil-Het (where L=mercaptothiazoline, mercaptopyridine or mercaptobenzothiazole). In the homogeneous route, the functionalization was achieved through a one-step reaction between the silica and an organic ligand containing the chelating functions; this gave the modified silicas denoted as L-Sil-Hom. The functionalized silicas were characterized by elemental analysis, IR spectroscopy and thermogravimetry. These materials were employed as adsorbents for mercury cations from aqueous and acetone solutions at room temperature. The results indicate that, in all cases, mercury adsorption was higher in the modified silicas prepared by the homogeneous method. (orig.)

  1. Characteristics and stability of mercury vapor adsorption over two kinds of modified semicoke.

    Science.gov (United States)

    Huawei, Zhang; Xiuli, Liu; Li, Wang; Peng, Liang

    2014-01-01

    In an attempt to produce effective and lower price gaseous Hg(0) adsorbents, two methods of HCl and KMnO4/heat treatment were used respectively for the surface modification of liginite semicoke from inner Mongolia. The different effects of modification process on the surface physical and chemical properties were analyzed. The characteristics and stability of mercury vapor adsorption over two kinds of modified semicoke were investigated. The results indicated that modification process caused lower micropore quantity and volume capacity of semicoke; the C-Cl functional groups, C=O bond and delocalized electron π on the surface of Cl-SC, the amorphous higher valency Mn (x+) , and O=C-OH functional groups on the surface of Mn-H-SC were the active sites for oxidation and adsorption of gaseous Hg(0). Modification process led to higher mercury removal efficiency of semicoke at 140°C and reduced the stability of adsorbed mercury of semicoke in simulated water circumstance simultaneously.

  2. Characteristics and Stability of Mercury Vapor Adsorption over Two Kinds of Modified Semicoke

    Directory of Open Access Journals (Sweden)

    Zhang Huawei

    2014-01-01

    Full Text Available In an attempt to produce effective and lower price gaseous Hg0 adsorbents, two methods of HCl and KMnO4/heat treatment were used respectively for the surface modification of liginite semicoke from inner Mongolia. The different effects of modification process on the surface physical and chemical properties were analyzed. The characteristics and stability of mercury vapor adsorption over two kinds of modified semicoke were investigated. The results indicated that modification process caused lower micropore quantity and volume capacity of semicoke; the C-Cl functional groups, C=O bond and delocalized electron π on the surface of Cl-SC, the amorphous higher valency Mnx+, and O=C–OH functional groups on the surface of Mn-H-SC were the active sites for oxidation and adsorption of gaseous Hg0. Modification process led to higher mercury removal efficiency of semicoke at 140°C and reduced the stability of adsorbed mercury of semicoke in simulated water circumstance simultaneously.

  3. Lead adsorption capacities of different components in natural surface coatings

    Institute of Scientific and Technical Information of China (English)

    DONG De-ming; HUA Xiu-yi; LI Yu; JI Liang; ZHANG Jing-jing

    2004-01-01

    Pb adsorption capacities of Fe oxide, Mn oxide and organic materials in natural surface coatings( biofilms and associated minerals) collected in three lakes, two ponds and a river in Jilin Province, China and Cayuga Lake in US were studied. A novel extraction technique was employed to remove one or more component(s) from the surface coatings. Pb adsorption to surface coatings before and after extraction was performed to determine the adsorptive properties of the extracted component(s). The statistical analysis of observed Pb adsorption was carried out using nonlinear least squares fitting(NLSF) to estimate the Pb adsorption capacity of each component of surface coatings. For each body of water, the estimated Pb adsorption capacity of Mn oxide(mol Pb/mol Mn) was significantly higher than that of Fe oxide( mol Pb/ mol Fe). The value of estimated adsorption capacities of organic materials with the unit mol Pb per kg COD was similar to or less than that of Fe oxides with the unit mol Pb per mol Fe. Comparison of components of surface coatings in different waters showed that the estimated Pb adsorption capacities of components in surface coatings developed in different natural waters were different,especially for Mn oxides.

  4. Synthesis, characterization, and mercury adsorption properties of hybrid mesoporous aluminosilicate sieve prepared with fly ash

    International Nuclear Information System (INIS)

    A novel hybrid mesoporous aluminosilicate sieve (HMAS) was prepared with fly ash and impregnated with zeolite A precursors. This improved the mercury adsorption of HMAS compared to original MCM-41. The HMAS was characterized by X-ray diffraction (XRD), nitrogen adsorption–desorption, Fourier transform infrared (FTIR) analysis, transmission electron microscopy (TEM) images and 29Si and 27Al magic angle spinning nuclear magnetic resonance (MAS NMR) spectra. These showed that the HMAS structure was still retained after impregnated with zeolite A. But the surface area and pore diameter of HMAS decreased due to pore blockage. Adsorption of mercury from aqueous solution was studied on untreated MCM-41and HMAS. The mercury adsorption rate of HMAS was higher than that of origin MCM-41. The adsorption of mercury was investigated on HMAS regarding the pH of mercury solution, initial mercury concentration, and the reaction temperature. The experimental data fit well to Langmuir and Freundlich isotherm models. The Dublin–Radushkevich isotherm and the characterization show that the mercury adsorption on HMAS involved the ion-exchange mechanisms. In addition, the thermodynamic parameters suggest that the adsorption process was endothermic in nature. The adsorption of mercury on HMAS followed the first order kinetics.

  5. Synthesis, characterization, and mercury adsorption properties of hybrid mesoporous aluminosilicate sieve prepared with fly ash

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Minmin [School of Environmental Science and Engineering, Tongji University, 1239 Siping Road, Shanghai 200092 (China); Hou, Li-an, E-mail: 11liuminmin@tongji.edu.cn [School of Environmental Science and Engineering, Tongji University, 1239 Siping Road, Shanghai 200092 (China); Xi, Beidou; Zhao, Ying; Xia, Xunfeng [China Research Academy of Environmental Science, Beijing 200012 (China)

    2013-05-15

    A novel hybrid mesoporous aluminosilicate sieve (HMAS) was prepared with fly ash and impregnated with zeolite A precursors. This improved the mercury adsorption of HMAS compared to original MCM-41. The HMAS was characterized by X-ray diffraction (XRD), nitrogen adsorption–desorption, Fourier transform infrared (FTIR) analysis, transmission electron microscopy (TEM) images and {sup 29}Si and {sup 27}Al magic angle spinning nuclear magnetic resonance (MAS NMR) spectra. These showed that the HMAS structure was still retained after impregnated with zeolite A. But the surface area and pore diameter of HMAS decreased due to pore blockage. Adsorption of mercury from aqueous solution was studied on untreated MCM-41and HMAS. The mercury adsorption rate of HMAS was higher than that of origin MCM-41. The adsorption of mercury was investigated on HMAS regarding the pH of mercury solution, initial mercury concentration, and the reaction temperature. The experimental data fit well to Langmuir and Freundlich isotherm models. The Dublin–Radushkevich isotherm and the characterization show that the mercury adsorption on HMAS involved the ion-exchange mechanisms. In addition, the thermodynamic parameters suggest that the adsorption process was endothermic in nature. The adsorption of mercury on HMAS followed the first order kinetics.

  6. [Simulation study on the effect of salinity on the adsorption behavior of mercury in wastewater-irrigated area].

    Science.gov (United States)

    Zheng, Shun-An; Li, Xiao-Hua; Xu, Zhi-Yu

    2014-05-01

    This study was designed to pinpoint the impact of salinity ( NaCl and Na2SO4, added at salinity levels of 0-5%, respectively) on the adsorption behavior of mercury in wastewater-irrigated areas of Tianjin City by batch and kinetic experiments. The results showed that, the Langmuir isotherm and the Elovich equation can well fitted batch and kinetic experimental data, respectively. As NaCI spiked in soil, Hg( II) adsorption capacity and strength had marked decreases, from 868.64 mgkg-1 and 1. 32 at control to 357.48 mgkg-1 and 0.63 at 5% salinity level of NaCI, respectively. As Na2SO4 spiked in soil, Hg(II) adsorption capacity (parameter qm in Langmuir isotherm) and strength (parameter k in Langmuir isotherm) changed slightly, from 868.64 mg kg-1 and 1.32 at control to 739.44 mg.kg-1 and 1. 18 at 5% salinity level of Na2 SO4, respectively. Kinetic data showed that, Hg( II) adsorption rate (parameter b in Elovich equation) in soil was not influenced by Na2SO, addition. However, the addition of NaC1 had a great effect on mercury adsorption rate. Hg(II ) adsorption capacity as a function of CI- or SO(2-)(4) content in soil could be simulated by the natural logarithm model, while Hg( II ) adsorption rate as a function of CI- content in soil could be simulated by the linear model. The study manifested that NaCI can significantly increase migration of Hg( II ) in the soil irrigated with wastewater, which may enhance Hg( II) bioavailability in the soil and cause a hazard to surface water. Especially, it will be harmful to human body through the food chain. PMID:25055690

  7. Evaluating the Adsorptive Capacities of Chemsorb 1000 and Chemsorb 1425

    Science.gov (United States)

    Monje, Oscar Alberto Monje; Surma, Jan M.; Johnsey, Marissa N.; Melendez, Orlando

    2014-01-01

    The Air Revitalization Lab at KSC tested Chemsorb 1000 and 1425, two candidate sorbents for use in future air revitalization technologies being evaluated by the ARREM project. Chemsorb 1000 and 1425 are granular coconut-shell activated carbon sorbents produced by Molecular Products, Inc. that may be used in the TCCS. Chemsorb 1000 is a high grade activated carbon for organic vapor adsorption. In contrast, Chemsorb 1425 is a high-grade impregnated activated carbon for adsorption of airborne ammonia and amines. Chemsorb 1000 was challenged with simulated spacecraft gas streams in order to determine its adsorptive capacities for mixtures of volatile organics compounds. Chemsorb 1425 was challenged with various NH3 concentrations to determine its adsorptive capacity.

  8. High capacity adsorption media and method of producing

    Science.gov (United States)

    Tranter, Troy J.; Mann, Nicholas R.; Todd, Terry A.; Herbst, Ronald S.

    2010-10-05

    A method of producing an adsorption medium to remove at least one constituent from a feed stream. The method comprises dissolving and/or suspending at least one metal compound in a solvent to form a metal solution, dissolving polyacrylonitrile into the metal solution to form a PAN-metal solution, and depositing the PAN-metal solution into a quenching bath to produce the adsorption medium. The at least one constituent, such as arsenic, selenium, or antimony, is removed from the feed stream by passing the feed stream through the adsorption medium. An adsorption medium having an increased metal loading and increased capacity for arresting the at least one constituent to be removed is also disclosed. The adsorption medium includes a polyacrylonitrile matrix and at least one metal hydroxide incorporated into the polyacrylonitrile matrix.

  9. Adsorption of mercury (II) from liquid solutions using modified activated carbons

    OpenAIRE

    Hugo Soé Silva; Silvia Virginia Ruiz; Dolly Lucía Granados; Juan Manuel Santángelo

    2010-01-01

    Mercury is one of the most toxic metals present in the environment. Adsorption has been proposed among the technologies for mercury abatement. Activated carbons are universal adsorbents which have been found to be a very effective alternative for mercury removal from water. The effectiveness with which a contaminant is adsorbed by the solid surface depends, among other factors, on the charge of the chemical species in which the contaminant is in solution and on the net charge of the adsorbent...

  10. Modeling and Experimental Studies of Mercury Oxidation and Adsorption in a Fixed-Bed Reactor

    Energy Technology Data Exchange (ETDEWEB)

    Buitrago, Paula A.; Morrill, Mike; Lighty, JoAnn S.; Silcox, Geoffrey D.

    2009-06-15

    This report presents experimental and modeling mercury oxidation and adsorption data. Fixed-bed and single-particle models of mercury adsorption were developed. The experimental data were obtained with two reactors: a 300-W, methane-fired, tubular, quartz-lined reactor for studying homogeneous oxidation reactions and a fixed-bed reactor, also of quartz, for studying heterogeneous reactions. The latter was attached to the exit of the former to provide realistic combustion gases. The fixed-bed reactor contained one gram of coconut-shell carbon and remained at a temperature of 150°C. All methane, air, SO2, and halogen species were introduced through the burner to produce a radical pool representative of real combustion systems. A Tekran 2537A Analyzer coupled with a wet conditioning system provided speciated mercury concentrations. At 150°C and in the absence of HCl or HBr, the mercury uptake was about 20%. The addition of 50 ppm HCl caused complete capture of all elemental and oxidized mercury species. In the absence of halogens, SO2 increased the mercury adsorption efficiency to up to 30 percent. The extent of adsorption decreased with increasing SO2 concentration when halogens were present. Increasing the HCl concentration to 100 ppm lessened the effect of SO2. The fixed-bed model incorporates Langmuir adsorption kinetics and was developed to predict adsorption of elemental mercury and the effect of multiple flue gas components. This model neglects intraparticle diffusional resistances and is only applicable to pulverized carbon sorbents. It roughly describes experimental data from the literature. The current version includes the ability to account for competitive adsorption between mercury, SO2, and NO2. The single particle model simulates in-flight sorbent capture of elemental mercury. This model was developed to include Langmuir and Freundlich isotherms, rate equations, sorbent feed rate, and

  11. Simultaneous Removal of NOx and Mercury in Low Temperature Selective Catalytic and Adsorptive Reactor

    Energy Technology Data Exchange (ETDEWEB)

    Neville G. Pinto; Panagiotis G. Smirniotis

    2006-03-31

    The results of a 18-month investigation to advance the development of a novel Low Temperature Selective Catalytic and Adsorptive Reactor (LTSCAR), for the simultaneous removal of NO{sub x} and mercury (elemental and oxidized) from flue gases in a single unit operation located downstream of the particulate collectors, are reported. In the proposed LTSCAR, NO{sub x} removal is in a traditional SCR mode but at low temperature, and, uniquely, using carbon monoxide as a reductant. The concomitant capture of mercury in the unit is achieved through the incorporation of a novel chelating adsorbent. As conceptualized, the LTSCAR will be located downstream of the particulate collectors (flue gas temperature 140-160 C) and will be similar in structure to a conventional SCR. That is, it will have 3-4 beds that are loaded with catalyst and adsorbent allowing staged replacement of catalyst and adsorbent as required. Various Mn/TiO{sub 2} SCR catalysts were synthesized and evaluated for their ability to reduce NO at low temperature using CO as the reductant. It has been shown that with a suitably tailored catalyst more than 65% NO conversion with 100% N{sub 2} selectivity can be achieved, even at a high space velocity (SV) of 50,000 h-1 and in the presence of 2 v% H{sub 2}O. Three adsorbents for oxidized mercury were developed in this project with thermal stability in the required range. Based on detailed evaluations of their characteristics, the mercaptopropyltrimethoxysilane (MPTS) adsorbent was found to be most promising for the capture of oxidized mercury. This adsorbent has been shown to be thermally stable to 200 C. Fixed-bed evaluations in the targeted temperature range demonstrated effective removal of oxidized mercury from simulated flue gas at very high capacity ({approx}>58 mg Hg/g adsorbent). Extension of the capability of the adsorbent to elemental mercury capture was pursued with two independent approaches: incorporation of a novel nano-layer on the surface of the

  12. Enhancing the adsorption of vapor-phase mercury chloride with an innovative composite sulfur-impregnated activated carbon.

    Science.gov (United States)

    Ie, Iau-Ren; Chen, Wei-Chin; Yuan, Chung-Shin; Hung, Chung-Hsuang; Lin, Yuan-Chung; Tsai, Hsieh-Hung; Jen, Yi-Shiu

    2012-05-30

    Mercury chloride (HgCl(2)) is the major mercury derivate emitted from municipal solid waste incinerators, which has high risk to the environment and human health. This study investigated the adsorption of vapor-phase HgCl(2) with an innovative composite sulfurized activated carbon (AC), which was derived from the pyrolysis, activation, and sulfurization of waste tires. The composite sulfur-impregnation process impregnated activated carbon with aqueous-phase sodium sulfide (Na(2)S) and followed with vapor-phase elemental sulfur (S(0)). Thermogravimetric analysis (TGA) was applied to investigate the adsorptive capacity of vapor-phase HgCl(2) using the composite sulfurized AC. The operating parameters included the types of composite sulfurized AC, the adsorption temperature, and the influent HgCl(2) concentration. Experimental results indicated that the sulfur-impregnation process could increase the sulfur content of the sulfurized AC, but decreased its specific surface area. This study further revealed that the composite sulfurized AC impregnated with aqueous-phase Na(2)S and followed with vapor-phase S(0) (Na(2)S+S(0) AC) had much higher saturated adsorptive capacity of HgCl(2) than AC impregnated in the reverse sequence (S(0)+Na(2)S AC). A maximum saturated adsorptive capacity of HgCl(2) up to 5236 μg-HgCl(2)/g-C was observed for the composite Na(2)S+S(0) AC, which was approximately 2.00 and 3.17 times higher than those for the single Na(2)S and S(0) ACs, respectively.

  13. Characteristic and mercury adsorption of activated carbon produced by CO2 of chicken waste

    Institute of Scientific and Technical Information of China (English)

    HUANG Yaji; JIN Baosheng; ZHONG Zhaoping; ZHONG Wenqi; XIAO Rui

    2008-01-01

    Preparation of activated carbon from chicken waste is a promising way to produce a useful adsorbent for Hg removal.A three-stage activation process (drying at 200℃,pyrolysis in N2 atmosphere,followed by CO2 activation) was used for the production of activated samples.The effects of carbonization temperature (400-600 ℃),activation temperature (700-900 ℃),and activation time (1-2.5 h) on the physicochemieal properties (weight-loss and BET surface) of the prepared carbon were investigated.Adsorptive removal of mercury from real flue gas onto activated carbon has been studied.The activated carbon from chicken waste has the same mercury capacity as commercial activated carbon (Darco LH) (HgV:38.7% vs.53.5%,HgO:50.5% vs.68.8%),although its surface area is around 10 times smaller,89.5 m2/g vs.862 m2/g.The low cost activated carbon can be produced from chicken waste,and the procedure is suitable.

  14. Mercury oxidation and adsorption characteristics of potassium permanganate modified lignite semi-coke

    Institute of Scientific and Technical Information of China (English)

    Huawei Zhang; Jitao Chen; Peng Liang; Li Wang

    2012-01-01

    The adsorption characteristics of virgin and potassium permanganate modified lignite semi-coke (SC) for gaseous Hg0 were investigated in an attempt to produce more effective and lower price adsorbents for the control of elemental mercury emission.Brunauer-Emmett-Teller (BET) measurements,X-ray powder diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) were used to analyze the surface physical and chemical properties of SC,Mn-SC and Mn-H-SC before and after mercury adsorption.The results indicated that potassium permanganate modification had significant influence on the properties of semi-coke,such as the specific surface area,pore structure and surface chemical functional groups.The mercury adsorption efficiency of modified semi-coke was lower than that of SC at low temperature,but much higher at high temperature.Amorphous Mn7+,Mn6+ and Mn4+ on the surface of Mn-SC and Mn-H-SC were the active sites for oxidation and adsorption of gaseous Hg0,which oxidized the elemental mercury into Hg2+ and captured it.Thermal treatment reduced the average oxidation degree of Mnx+ on the surface of Mn-SC from 3.80 to 3.46.However,due to the formation of amorphous MnOx,the surface oxidation active sites for gaseous Hg0 increased,which gave Mn-H-SC higher mercury adsorption efficiency than that of Mn-SC at high temperature.

  15. Silver impregnated carbon for adsorption and desorption of elemental mercury vapors

    Institute of Scientific and Technical Information of China (English)

    Despina Karatza; Marina Prisciandaro; Amedeo Lancia; Dino Musmarra

    2011-01-01

    The Hg0 vapor adsorption experimental results on a novel sorbent obtained by impregnating a commercially available activated carbon (Darco G60 from BDH) with silver nitrate were reported.The study was performed by using a fundamental approach,in an apparatus at laboratory scale in which a synthetic flue gas,formed by Hg0 vapors in a nitrogen gas stream,at a given temperature and mercury concentration,was flowed through a fixed bed of adsorbent material.Breakthrough curves and adsorption isotherms were obtained for bed temperatures of 90,120 and 150°C and for Hg0 concentrations in the gas varying in the range of 0.8-5.0 mg/m3.The experimental gas-solid equilibrium data were used to evaluate the Langmuir parameters and the heat of adsorption.The experimental results showed that silver impregnated carbon was very effective to capture elemental mercury and the amount of mercury adsorbed by the carbon decreased as the bed temperature increased.In addition,to evaluate the possibility of adsorbent recovery,desorption was also studied.Desorption runs showed that both the adsorbing material and the mercury could be easily recovered,since at the end of desorption the residue on solid was almost negligible.The material balance on mercury and the constitutive equations of the adsorption phenomenon were integrated,leading to the evaluation of only one kinetic parameter which fits well both the experimentally determined breakthrough and desorption curves.

  16. Effect of calcium on adsorption capacity of powdered activated carbon.

    Science.gov (United States)

    Li, Gang; Shang, Junteng; Wang, Ying; Li, Yansheng; Gao, Hong

    2013-12-01

    We investigated the effect of calcium ion on the adsorption of humic acid (HA) (as a target pollutant) by powered activated carbon. The HA adsorption isotherms at different pH and kinetics of two different solutions including HA alone and HA doped Ca(2+), were performed. It was showed that the adsorption capacity of powdered activated carbon (PAC) for HA was markedly enhanced when Ca(2+) was doped into HA. Also, HA and Ca(2+) taken as nitrate were tested on the uptake of each other respectively and it was showed that the adsorbed amounts of both of them were significantly promoted when HA and calcium co-existed. Furthermore, the adsorbed amount of HA slightly decreased with the increasing of Ca(2+) concentration, whereas the amount of calcium increased with the increasing of HA concentration, but all above the amounts without addition. Finally, the change of pH before and after adsorption process is studied. In the two different solutions including HA alone and HA doped Ca(2+), pH had a small rise, but the extent of pH of later solution was bigger. PMID:25078809

  17. MERCURY ADSORPTION BY ARTHOBACTER GLOBIFORMIS AND SPIRULINA PLATENSIS

    Directory of Open Access Journals (Sweden)

    T. L. Kalabegishvili

    2011-06-01

    Full Text Available The increasing contamination of soil, sediment, and water with heavy metals by natural and industrial processes is a worldwide problem. Many bacteria and microalgae have demonstrated ability to absorb toxic elements. To study mercury biosorption by bacteria Arthrobacter globiformis and microalga Spirulina platensis neutron activation analysis (NAA was applied. The process of mercury biosorption by these media was described by Freundlich and Langmuir-Freundlich Model. Both microorganisms showed a great potential to be used as biosorbing agents for mercury removal from the environment.

  18. Study on characteristics of elemental mercury adsorption by bamboo charcoal%竹炭脱除单质汞的特性研究

    Institute of Scientific and Technical Information of China (English)

    谭增强; 邱建荣; 苏胜; 向军

    2012-01-01

    为了寻求廉价、高效的脱汞吸附剂,总结了竹炭的来源、制备方法、竹炭(BC)的性质以及竹炭的应用现状,并将其应用在燃煤大气污染物汞的脱除上.在小型燃煤烟气汞脱除实验台上和模拟烟气气氛下研究了低温下BC对汞吸附性能的影响因素.实验结果表明:BC对汞有较强的吸附能力,BC粒径减小增大了BC表面积和孔容,这有利于物理吸附脱汞;吸附剂质量与流量比值(W/F)的增加延长了汞与BC的接触时间,非常利于汞的吸附脱除;BC的脱汞效率随汞浓度的增大而降低;BC对汞的吸附脱除存在着最佳反应温度,实验发现60℃为最佳脱除温度;氧气会促进单质汞的氧化,从而进一步提高BC脱除汞的能力.%The purpose of the present study was to develop cost-effective carbon-based sorbent using commercial bamboo charcoal (BC) which was produced from renewable bamboo precursor. The source, preparation methods, properties and application status of bamboo charcoal were summarized. The adsorptive potential of BC for elemental mercury was investigated through a parametric study conducted with a bench-scale bed. The effect of temperature, W/F, initial concentration and oxygen on mercury removal were analyzed. The results show that BC has strong adsorption capacity for mercury. The decrease of particle size of BC increases its BET surface area and pore volume, which can enhance its physisorption ability for elemental mercury. The increase of W/F prolongs the residence time of elemental mercury, thus improves the removal efficiency of elemental mercury. The increase of concentration of inlet mercury decreases the removal efficiency of elemental mercury. There is a best reaction temperature for the adsorption of mercury, and 60 ℃ is found to be the optimal reaction temperature. The presence of oxygen can oxidize elemental mercury and further increase the adsorption ability for

  19. Dynamic measurement of mercury adsorption and oxidation on activated carbon in simulated cement kiln flue gas

    DEFF Research Database (Denmark)

    Zheng, Yuanjing; Jensen, Anker Degn; Windelin, Christian;

    2012-01-01

    of the sulfite converter is short and typically within 2min. Dynamic mercury adsorption and oxidation tests on commercial activated carbons Darco Hg and HOK standard were performed at 150°C using simulated cement kiln gas and a fixed bed reactor system. It is shown that the converter and analyzer system...

  20. Removal of Mercury(II from Aqueous Solutions by Adsorption on Poly(1-amino-5-chloroanthraquinone Nanofibrils: Equilibrium, Kinetics, and Mechanism Studies

    Directory of Open Access Journals (Sweden)

    Shaojun Huang

    2016-01-01

    Full Text Available Poly(1-amino-5-chloroanthraquinone (PACA nanofibrils were applied as novel nanoadsorbents for highly toxic mercury removal from aqueous solutions. A series of batch adsorption experiments were conducted to study the effect of adsorbent dose, pH, contact time, and metal concentration on Hg(II uptake by PACA nanofibrils. Kinetic data indicated that the adsorption process of PACA nanofibrils for Hg(II achieved equilibrium within 2 h following a pseudo-second-order rate equation. The adsorption mechanism of PACA nanofibrils for Hg(II was investigated by Fourier transform-infrared (FT-IR spectra and X-ray photoelectron spectroscopy (XPS analyses. The adsorption isotherm of Hg(II fitted well the Langmuir model, exhibiting superb adsorption capacity of 3.846 mmol of metal per gram of adsorbent. Lastly, we found out that the as-synthesized PACA nanofibrils are efficient in Hg(II removal from real wastewater. Furthermore, five consecutive adsorption-desorption cycles demonstrated that the PACA nanofibrils were suitable for repeated use without considerable changes in the adsorption capacity.

  1. Oxygen Storage Capacity and Adsorptive Property of Praseodymium Oxides

    Institute of Scientific and Technical Information of China (English)

    万颖; 马建新; 方明; 刘毅廷

    2003-01-01

    Oxygen storage and adsorptive properties of praseodymium oxides were investigated by pulse experiments and temperature-programmed desportion/reduction (TPD/TPR) experiments. Pr2O3 possesses the similar oxygen storage properties to CeO 2, and its dynamic oxygen storage capacity is 14.9 μmolg-1. The studies on TPD of O2, H2O and CO and TPR show that Pr2O3 provides more active sur face oxygen species and at a lower temperature than CeO2. It is suggested that Pr2O3 can be a well candidate as an oxygen storage component in automobile three-way catalyst.

  2. Determination of mercury in discharge water from plastic manufactory by neutron activation analysis and copper powder adsorption

    International Nuclear Information System (INIS)

    Through copper powder adsorption, neutron activation analysis was used to determine the mercury in discharge water from a plastic manufactory where the water samples were taken from various discharge ditches. The experimental results showed that waste water from mercury cells contained 1.7x10-9 approximately 8.19x10-6 g Hg/ml while water samples taken from other areas did not show significant mercury level and were below the limit of detection. (author)

  3. Sulfide treatment to inhibit mercury adsorption onto activated carbon in carbon-in-pulp gold recovery circuits

    Energy Technology Data Exchange (ETDEWEB)

    Touro, F.J.; Lipps, D.A.

    1988-03-29

    A process for treating a mercury-contaminated, precious metal-containing ore slurry is described comprising: (a) reacting sulfide anions in an aqueous ore slurry of a mercury and precious metal-containing carbonaceous ore, and (b) conducting a simultaneous cyanide leach and carbon-in-pulp adsorption of the precious metal from the carbonaceous ore in the sulfide-containing ore slurry.

  4. Adsorption of mercury on lignin: Combined surface complexation modeling and X-ray absorption spectroscopy studies

    International Nuclear Information System (INIS)

    Adsorption of mercury (Hg) on lignin was studied at a range of pH values using a combination of batch adsorption experiments, a surface complexation model (SCM) and synchrotron X-ray absorption spectroscopy (XAS). Surface complexation modeling indicates that three types of acid sites on lignin surfaces, namely aliphatic carboxylic-, aromatic carboxylic- and phenolic-type surface groups, contributed to Hg(II) adsorption. The bond distance and coordination number of Hg(II) adsorption samples at pH 3.0, 4.0 and 5.5 were obtained from extended X-ray absorption fine structure (EXAFS) spectroscopy analysis. The results of SCM and XAS combined reveal that the predominant adsorption species of Hg(II) on lignin changes from HgCl20 to monodentate complex –C–O–HgCl and then bidentate complex –C–O–Hg–O–C– with increasing pH value from 2.0 to 6.0. The good agreement between SCM and XAS results provides new insight into understanding the mechanisms of Hg(II) adsorption on lignin. - Highlights: ► Lignin exhibits a high Hg(II) adsorption capability. ► Adsorption of Hg(II) on lignin is strongly pH-dependent. ► HgCl20, –C–O–HgCl and –C–O–Hg–O–C– are the main adsorption species of Hg(II). - Adsorption of Hg(II) on lignin is strongly pH-dependent, and the main adsorption Hg(II) species change from HgCl20 to –C–O–HgCl and –C–O–Hg–O–C– as pH increases from 2.0 to 6.0.

  5. Mercury

    International Nuclear Information System (INIS)

    Papers are presented on future observations of and missions to Mercury, the photometry and polarimetry of Mercury, the surface composition of Mercury from reflectance spectrophotometry, the Goldstone radar observations of Mercury, the radar observations of Mercury, the stratigraphy and geologic history of Mercury, the geomorphology of impact craters on Mercury, and the cratering record on Mercury and the origin of impacting objects. Consideration is also given to the tectonics of Mercury, the tectonic history of Mercury, Mercury's thermal history and the generation of its magnetic field, the rotational dynamics of Mercury and the state of its core, Mercury's magnetic field and interior, the magnetosphere of Mercury, and the Mercury atmosphere. Other papers are on the present bounds on the bulk composition of Mercury and the implications for planetary formation processes, the building stones of the planets, the origin and composition of Mercury, the formation of Mercury from planetesimals, and theoretical considerations on the strange density of Mercury

  6. Alkali metal cation doping of metal-organic framework for enhancing carbon dioxide adsorption capacity

    Institute of Scientific and Technical Information of China (English)

    Yan Cao; Yunxia Zhao; Fujiao Song; Qin Zhong

    2014-01-01

    Metal-organic frameworks (MOFs) have attracted much attention as adsorbents for the separation of CO2 from flue gas or natural gas. Here, a typical metal-organic framework HKUST-1(also named Cu-BTC or MOF-199) was chemically reduced by doping it with alkali metals (Li, Na and K) and they were further used to investigate their CO2 adsorption capacities. The structural information, surface chemistry and thermal behavior of the prepared adsorbent samples were characterized by X-ray powder diffraction (XRD), thermo-gravimetric analysis (TGA) and nitrogen adsorption-desorption isotherm analysis. The results showed that the CO2 storage capacity of HKUST-1 doped with moderate quantities of Li+, Na+ and K+, individually, was greater than that of unmodified HKUST-1. The highest CO2 adsorption uptake of 8.64 mmol/g was obtained with 1K-HKUST-1, and it was ca. 11%increase in adsorption capacity at 298 K and 18 bar as compared with HKUST-1. Moreover, adsorption tests showed that HKUST-1 and 1K-HKUST-1 displayed much higher adsorption capacities of CO2 than those of N2. Finally, the adsorption/desorption cycle experiment revealed that the adsorption performance of 1K-HKUST-1 was fairly stable, without obvious deterioration in the adsorption capacity of CO2 after 10 cycles.

  7. Adsorption Capacity of Kaolinite for Copper (II) under Magnetic Field

    Institute of Scientific and Technical Information of China (English)

    DONG Wei

    2004-01-01

    The adsorption of Cu2+ on kaolinite under magnetic field was studied at 25℃.The magnetic effects were investigated by designing the variation of exposure time,magnetic flux density and the method of magnetic exposure.The results from these study show that the magnetic treatment significantly enhance the fraction of adsorption of Cu2+,the adsorption of Cu2+ by kaolinite increases with the increase of pH value from 2 to 6.Both the magnetic exposure time and the magnetic flux density promote the fraction of adsorption Cu2+ on kaolinite.

  8. Studies on The Adsorption Capacity for Bilirubin of The Adsorbent Chitosan-β-Cyclodextrin

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The adsorbent crosslinked chitosan-β-cyclodextrin (β-CD) was prepared by the reaction of glutaraldehyde with chitosan and β-cyclodextrin. This type of adsorbent has high adsorption capacity for unconjugated bilirubin. The adsorption capacity was related to the β-CD content of the adsorbent; phosphate buffer concentration; temperature; pH value; ionic strength and the adsorbent beads. The results indicated that the chitosan-β-CD was a good adsorbent for unconjugated bilirubin with high capacity.

  9. Removal of mercury(II) ions in aqueous solution using the peel biomass of Pachira aquatica Aubl: kinetics and adsorption equilibrium studies.

    Science.gov (United States)

    Santana, Andrea J; dos Santos, Walter N L; Silva, Laiana O B; das Virgens, Cesário F

    2016-05-01

    Mercury is a highly toxic substance that is a health hazard to humans. This study aims to investigate powders obtained from the peel of the fruit of Pachira aquatica Aubl, in its in natura and/or acidified form, as an adsorbent for the removal of mercury ions in aqueous solution. The materials were characterized by Fourier transform infrared spectroscopy and thermogravimetric analysis. The infrared spectra showed bands corresponding to the axial deformation of carbonyls from carboxylic acids, the most important functional group responsible for fixing the metal species to the adsorbent material. The thermograms displayed mass losses related to the decomposition of three major components, i.e., hemicellulose, cellulose, and lignin. The adsorption process was evaluated using cold-vapor atomic fluorescence spectrometry (CV AFS) and cold-vapor atomic absorption spectrometry (CV AAS). Three isotherm models were employed. The adsorption isotherm model, Langmuir-Freundlich, best represented the adsorption process, and the maximum adsorption capacity was predicted to be 0.71 and 0.58 mg g(-1) at 25 °C in nature and acidified, respectively. Adsorption efficiencies were further tested on real aqueous wastewater samples, and removal of Hg(II) was recorded as 69.6 % for biomass acidified and 76.3 % for biomass in nature. Results obtained from sorption experiments on real aqueous wastewater samples revealed that recovery of the target metal ions was very satisfactory. The pseudo-second-order model showed the best correlation to the experimental data. The current findings showed that the investigated materials are potential adsorbents for mercury(II) ion removal in aqueous solution, with acidified P. aquatica Aubl being the most efficient adsorbent.

  10. Removal of mercury(II) ions in aqueous solution using the peel biomass of Pachira aquatica Aubl: kinetics and adsorption equilibrium studies.

    Science.gov (United States)

    Santana, Andrea J; dos Santos, Walter N L; Silva, Laiana O B; das Virgens, Cesário F

    2016-05-01

    Mercury is a highly toxic substance that is a health hazard to humans. This study aims to investigate powders obtained from the peel of the fruit of Pachira aquatica Aubl, in its in natura and/or acidified form, as an adsorbent for the removal of mercury ions in aqueous solution. The materials were characterized by Fourier transform infrared spectroscopy and thermogravimetric analysis. The infrared spectra showed bands corresponding to the axial deformation of carbonyls from carboxylic acids, the most important functional group responsible for fixing the metal species to the adsorbent material. The thermograms displayed mass losses related to the decomposition of three major components, i.e., hemicellulose, cellulose, and lignin. The adsorption process was evaluated using cold-vapor atomic fluorescence spectrometry (CV AFS) and cold-vapor atomic absorption spectrometry (CV AAS). Three isotherm models were employed. The adsorption isotherm model, Langmuir-Freundlich, best represented the adsorption process, and the maximum adsorption capacity was predicted to be 0.71 and 0.58 mg g(-1) at 25 °C in nature and acidified, respectively. Adsorption efficiencies were further tested on real aqueous wastewater samples, and removal of Hg(II) was recorded as 69.6 % for biomass acidified and 76.3 % for biomass in nature. Results obtained from sorption experiments on real aqueous wastewater samples revealed that recovery of the target metal ions was very satisfactory. The pseudo-second-order model showed the best correlation to the experimental data. The current findings showed that the investigated materials are potential adsorbents for mercury(II) ion removal in aqueous solution, with acidified P. aquatica Aubl being the most efficient adsorbent. PMID:27084802

  11. Experimental Investigation on Adsorption Capacity of a Variety of Activated Carbon/Refrigerant Pairs

    Directory of Open Access Journals (Sweden)

    Ahmed N. Shmroukh

    2015-04-01

    Full Text Available This study aims to develop a device with minimum heat and mass transfer limitations between adsorbent and adsorbate, and subsequently to obtain practically applicable adsorption capacity data. Also, 5 kW adsorption chillers (evaporators, condensers and adsorbers are designed based on the experimental output data of the whole tested pairs. A finned-tube heat exchanger was employed and installed at the center adsorber, and each employed adsorbent was immobilized on its surfaces by using an adhesive agent. A variety of pairs: are activated carbon powder (ACP/R-134a, ACP/R-407c, ACP/R-507A, activated carbon granules (ACG/R-507A, ACG /R-407c and ACG /R-134a, were examined at different adsorption temperatures of 25, 30, 35 and 50°C. It was found that, at the adsorption temperature of 25°C the maximum adsorption capacity was 0.8352 kg kg-1 for ACP/R-134a, while at the adsorption temperature of 50°C the maximum adsorption capacity was 0.3207 kg kg-1 for ACP/R- 134a. Therefore, the ACP/R-134a pair is highly recommended to be employed as adsorption refrigeration working pair because of its higher maximum adsorption capacity higher than the other examined pairs.

  12. Capability of defective graphene-supported Pd13 and Ag13 particles for mercury adsorption

    Science.gov (United States)

    Meeprasert, Jittima; Junkaew, Anchalee; Rungnim, Chompoonut; Kunaseth, Manaschai; Kungwan, Nawee; Promarak, Vinich; Namuangruk, Supawadee

    2016-02-01

    Reactivity of single-vacancy defective graphene (DG) and DG-supported Pdn and Agn (n = 1, 13) for mercury (Hg0) adsorption has been studied using density functional theory calculation. The results show that Pdn binds defective site of DG much stronger than the Agn, while metal nanocluster binds DG stronger than single metal atom. Metal clustering affects the adsorption ability of Pd composite while that of Ag is comparatively less. The binding strength of -8.49 eV was found for Pd13 binding on DG surface, indicating its high stability. Analyses of structure, energy, partial density of states, and d-band center (ɛd) revealed that the adsorbed metal atom or cluster enhances the reactivity of DG toward Hg adsorption. In addition, the Hg adsorption ability of Mn-DG composite is found to be related to the ɛd of the deposited Mn, in which the closer ɛd of Mn to the Fermi level correspond to the higher adsorption strength of Hg on Mn-DG composite. The order of Hg adsorption strength on Mn-DG composite are as follows: Pd13 (-1.68 eV) >> Ag13 (-0.67 eV) ∼ Ag1 (-0.69 eV) > Pd1 (-0.62 eV). Pd13-DG composite is therefore more efficient sorbent for Hg0 removal in terms of high stability and high adsorption reactivity compared to the Ag13. Further design of highly efficient carbon based sorbents should be focused on tailoring the ɛd of deposited metals.

  13. Mercury

    Science.gov (United States)

    ... equipment Inorganic mercury can be found in: Batteries Chemistry labs Some disinfectants Folk remedies Red cinnabar mineral ... the lungs Medicine to remove mercury and heavy metals from the body INORGANIC MERCURY For inorganic mercury ...

  14. Study of Static Adsorption Capacity of ACF for Xenon at 201 K

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The static adsorption performances of a series of active carbon fiber (ACF)for xenon at 201 K were measured with a model ASAP2010M specific surface area and aperture distribution instrument by changing the working gas of instrument from N2 to Xenon. Compared with grain active carbon(GAC): (1) the adsorption performance of Viscose-based ACF(VACF) adsorbents is better than that of GAC; (2) owing to the difference of aperture distribution, the adsorption performance of ACF with different radicales is different under the same experiment conditions though the specific surface area is similar; (3) there is no definite relationship between adsorption performance and specific surface area; (4) the VACF-A2 is the superior xenon adsorbent at the experimental temperature.Keyworls Active carbon fiber, CTBT, Xenon, Static adsorption, Adsorptive capacity, Adsorptive velocity

  15. Adsorption capacity of various adsorbents for decolorization of wastewater

    OpenAIRE

    Romčević, Gorana

    2014-01-01

    Adsorption is applied for the removal of dyes from wastewater effluent from textile and other industries. Dyes from wastewater need to be removed before it mixes with water bodies. Among the treatment options, adsorption appears to have considerable potential for the removal of colour from wastewaters. Activated carbon is the most widely used adsorbent, but its use is limited due to its high cost. This cost problem has led to a search for the use of alternate cheap and efficient materials. ...

  16. Modeling high adsorption capacity and kinetics of organic macromolecules on super-powdered activated carbon.

    Science.gov (United States)

    Matsui, Yoshihiko; Ando, Naoya; Yoshida, Tomoaki; Kurotobi, Ryuji; Matsushita, Taku; Ohno, Koichi

    2011-02-01

    The capacity to adsorb natural organic matter (NOM) and polystyrene sulfonates (PSSs) on small particle-size activated carbon (super-powdered activated carbon, SPAC) is higher than that on larger particle-size activated carbon (powdered-activated carbon, PAC). Increased adsorption capacity is likely attributable to the larger external surface area because the NOM and PSS molecules do not completely penetrate the adsorbent particle; they preferentially adsorb near the outer surface of the particle. In this study, we propose a new isotherm equation, the Shell Adsorption Model (SAM), to explain the higher adsorption capacity on smaller adsorbent particles and to describe quantitatively adsorption isotherms of activated carbons of different particle sizes: PAC and SPAC. The SAM was verified with the experimental data of PSS adsorption kinetics as well as equilibrium. SAM successfully characterized PSS adsorption isotherm data for SPACs and PAC simultaneously with the same model parameters. When SAM was incorporated into an adsorption kinetic model, kinetic decay curves for PSSs adsorbing onto activated carbons of different particle sizes could be simultaneously described with a single kinetics parameter value. On the other hand, when SAM was not incorporated into such an adsorption kinetic model and instead isotherms were described by the Freundlich model, the kinetic decay curves were not well described. The success of the SAM further supports the adsorption mechanism of PSSs preferentially adsorbing near the outer surface of activated carbon particles. PMID:21172719

  17. Structural properties and adsorption capacity of holocellulose aerogels synthesized from an alkali hydroxide-urea solution

    Energy Technology Data Exchange (ETDEWEB)

    Kwon, Gu-Joong; Kim, Dae-Young; Hwang, Jae-Hyun; Kang, Joo-Hyon [Dongguk University, Seoul (Korea, Republic of)

    2014-05-15

    A tulip tree was used to synthesize a holocellulose aerogel from an aqueous alkali hydroxide-urea solution with the substitution of an organic solvent followed by freeze-drying. For comparison, the synthesized holocellulose aerogels were divided into two groups according to the source of the hydrogel, an upper suspended layer and a bottom concentrated layer of the centrifuged solution of cellulose and NaOH/urea solvents. We investigated the effects of the temperature of the pre-cooled NaOH/urea solution (i.e., dissolution temperature) on the pore structure and the adsorption capacity of the holocellulose aerogel. A nano-fibrillar network structure of the holocellulose aerogel was observed, with little morphological difference in pore structure for different dissolution temperatures. Both micropores and mesopores were observed in the holocellulose aerogel. The specific surface area of the holocellulose aerogel was generally greater at lower dissolution temperatures. In a series of adsorption tests using methylene blue, the holocellulose aerogel showed the greatest adsorption capacity at the lowest dissolution temperature tested ( -2 .deg. C). However, the dissolution temperature generally had little effect on the adsorption capacity. The holocellulose aerogel produced from the upper suspended layer of the centrifuged hydrogel solution showed a greater porosity and adsorption capacity than the one produced from the bottom concentrated layer. Overall, the aerogel made by utilizing a delignified tulip tree display a high surface area and a high adsorption property, indicating its possible application in eco-friendly adsorption materials.

  18. Adsorption-Desorption Characteristics of Inorganic Mercury and Methyl Mercury in Soils%无机汞和甲基汞在土壤中的吸附-解吸特性研究

    Institute of Scientific and Technical Information of China (English)

    陈宁; 陈艳; 田超; 司友斌

    2013-01-01

    Adsorption-desorption of inorganic mercury (HgCl2) and Methyl mercury (MeHg) in four different soils and the effects of pH on the adsorption were studied using batch equilibration techniques.The results showed that the adsorption-desorption isotherms of HgCl2 and MeHg in soils were fitted by the Freundlich empirical equation(r>0.98).The adsorption coefficients Kf of HgCl2 in paddy soil,red soil,yellow brown soil,shajiang black soil were 122.25,86.60,70.95,76.60,respectively; The Kf values of MeHg were 55.99,45.00,41.94,40.43,respectively.The soils had the great adsorption capacity for HgCl2 and MeHg,and soil adsorption for HgCl2 was stronger than that for MeHg.The adsorption of HgCl2 and MeHg in soils increased with increase in the organic matter contents of the soil.The changes of soil initial pHcould influence the adsorption of HgCl2,and the largest amount of adsorption took place under neutral conditions,but it had little effect on the adsorption of MeHg.The desorption of HgCl2 and MeHg from soils showed significant hysteresis effects which was indicated by the higher adsorption slope (1/nads) compared to the desorption slope(1/nads).Soils that adsorbed more mercury also desorbed less mercury.%采用振荡平衡法,研究了无机汞和甲基汞在4种土壤中的吸附-解吸规律及其pH对汞吸附的影响.结果表明:无机汞和甲基汞在土壤中的吸附-解吸均符合Freundlich方程;无机汞在水稻土、红壤、黄褐土、砂姜黑土中吸附的Kf值分别为122.25、86.60、70.95、76.60,甲基汞为55.99、45.00、41.94、40.43.土壤对两种汞均有较强的吸附能力,且土壤对无机汞的吸附能力强于甲基汞.有机质含量越高的土壤,对汞的吸附能力越强;改变土壤初始pH对无机汞的吸附具有一定的影响,过酸或过碱环境不利于土壤对无机汞的吸附,但土壤初始pH变化对甲基汞的吸附影响不大.无机汞和甲基汞在土壤中的解吸过程都存在明显的滞后效

  19. A new methodology to evaluate adsorption capacity on nanomaterials

    International Nuclear Information System (INIS)

    Nanomaterials preparation has undergone great development in recent years, with important applications. The adsorbent properties of these nanomaterials cannot be always done using batch studies, because the nanometric particle size often hinders its physical separation, and this may affect the conclusions regarding adsorption studies. A new and simple method was developed, based on electrochemical measurements. For the validation process, synthetic alumina was used as adsorbent with copper solutions. The solid/solution ratio was kept constant in both the electrochemical and batch methods, optimizing in each case the adsorption equilibration time. Peak current versus Cu2+ concentration linearity was assessed from voltammograms. The electrochemical adsorption was accomplished utilizing cyclic voltammetry before and after the addition of the adsorbent. The amount of sorbed element was determined from the difference between the amount of Cu2+ added and that present in solution at equilibrium. The Langmuir, Freundlich, and Langmuir–Freundlich models were used to fit the experimental data obtained by both methods. The results of the electrochemical methodology have precision and accuracy statistically comparable to those obtained with the batch method. The electrochemical technique has the advantage of shorter adsorbent/adsorbate equilibration times than batch and do not require physical separation, allowing the adsorption on the imogolite to be established

  20. Study on the adsorption capacity for mercury (Ⅱ) with chromium/cobaIt-doped graphene oxide materiaIs%负载铬钴石墨烯基材料对汞(Ⅱ)的吸附性能研究

    Institute of Scientific and Technical Information of China (English)

    王卓; 邓娟; 朱君妍; 周超; 周晓吉; 郭永福; 白仁碧

    2016-01-01

    The chromium and cobalt doped reduced graphene oxide (RGO/Cr,RGO/Co) composite materials have been synthesized by making use of the reducibility of RGO and the oxidability of transition metallic salts ,and app-lied to the adsorption for Hg2+. The results show that the specific surface area of RGO/Cr is higher than that of RGO/Co and RGO. The hydrophilicity of RGO is effectively improved after having been doped with chromium or cobalt. The theoretical monolayer adsorption capacities of RGO,RGO/Cr and RGO/Co fitting Langmuir model are 128.98,181.86, and 146.86 mg/g,respectively,and the adsorption processes of these three materials complies with the pseudo-first-order and pseudo-second-order kinetic model.%利用石墨烯的还原性与过渡金属盐类的氧化性,制备得到分别负载有铬和钴的还原氧化石墨烯(RGO)复合材料RGO/Cr和RGO/Co,并将其应用于对Hg2+的吸附。结果表明:RGO/Cr比RGO/Co及RGO具有更大比表面积,负载铬和钴后RGO的亲水性能显著增加。 Langmuir拟合RGO、RGO/Cr、RGO/Co对Hg2+的理论单层最大吸附容量分别为128.98、181.86、146.86 mg/g,同时吸附过程均符合伪一级和伪二级动力学模型。

  1. Efficient removal and highly selective adsorption of Hg2+ by polydopamine nanospheres with total recycle capacity

    International Nuclear Information System (INIS)

    Highlights: • The PDA nanospheres with uniform diameter of 150–200 nm were used to remove Hg2+ efficiently and selectively. • The desorption capacity of PDA nanospheres was 100% in pH 1. • The structure and removal capacity of PDA nanospheres remained almost unchanged after recycling five times. - Abstract: This study reported a new method for efficient removal of Hg2+ from contaminated water using highly selective adsorptive polydopamine (PDA) nanospheres, which were uniform and had a small diameter (150–200 nm). The adsorption isotherms, kinetics, thermodynamics were investigated. Also, the effects of ionic strength, co-existing ions on removing ability of PDA nanospheres for Hg2+ were studied. Adsorption of Hg2+ was very fast and efficient as adsorption equilibrium was completed within 4 h and the maximum adsorption capacities were 1861.72 mg/g, 2037.22 mg/g, and 2076.81 mg/g at 298 K, 313 K, and 328 K respectively, increasing with increasing of temperature. The PDA nanospheres exhibited highly selective adsorption of Hg2+ and had a total desorption capacity of 100% in hydrochloric acid solution, pH 1. The results showed that the structure of PDA nanospheres remained almost unchanged after recycling five times. Furthermore, X-ray photoelectron spectroscopy (XPS) was employed to determine the elements of PDA nanospheres before and after Hg2+ adsorption. Considering their efficient and highly Hg2+ selective adsorption, total recycle capacity, and high stability, PDA nanospheres will be feasible in a number of practical applications

  2. Effect of dissolved organic matter on adsorption and desorption of mercury by soils

    Institute of Scientific and Technical Information of China (English)

    YANG Yongkui; LIANG Li; WANG Dingyong

    2008-01-01

    Effects of dissolved organic matter (DOM) on adsorption and desorption of Hg were investigated in two kinds of soils, Xanthi-Udic Ferralosols (XUF) and Typic Purpli-Udic Cambosols (TPUC). The DOM was obtained from humus soil (DOMH), rice straw (DOMR), and pig manure (DOMP). The presence of DOM obviously reduced Hg maximum adsorption capacity with up to 40% decreases over the control, being an order of DOMH (250.00 mg/kg) (270.27 mg/kg) (312.50 mg/kg) adsorption was slightly weaker in XUF than in TPUC. Meanwhile, the DOM promoted Hg desorption from the soils. The kinetic models, the Two-constant equation and Elovich equation, were applicable to describe the adsorption and desorption processes of Fig in soils. The speed of Hg adsorption was consistently slowed down by the existence of DOM..

  3. Mass transfer and kinetic studies on mercury adsorption by titania nanofibers

    Directory of Open Access Journals (Sweden)

    Dixit Abhilasha

    2016-01-01

    Full Text Available The stringent laws and tight regulation on heavy metal bearing wastewaters being discharged into the water stream lead to emergence of technically advanced and super effective treatment methods. Heavy metal contaminated aqueous streams have become a global concern due to their carcinogenicity and delirious effects on human health. In particular, the health hazards of mercury include adverse effect on central nervous system, pulmonary and kidney functions, etc. Having a maximum discharge limit of 0.001 mg/L, which is the lowest amongst other heavy metals, mercury contamination has become a matter of global concern. In the present study, TiO2 having a proven track record for its affinity for heavy metals was lab synthesized in the form of fiber mats and tested for its adsorptive behaviour towards Hg(II in aqueous system. The electrospinned nanofibers possessed smooth morphology and very high surface area ≈ 740 m2/g. The batch adsorption experiments showed titania nanofibers possessed great affinity towards Hg(II. At the most optimized conditions the removal percentage went remarkably high to 95.5% with initial Hg(II concentration of 0.01 mg/L. Since the rate limiting steps in adsorption are of vital importance in order to define the rate parameters for design purposes, the present study takes into account External mass transfer, Weber and Morris and Boyd mass transfer diffusion models for Hg(II adsorption on lab synthesized titania nanofibers. The equilibrium data were then analyzed using Langmuir, Freundlich and Temkin sorption models and the characteristic sorption parameters for each isotherm were determined. The Mass transfer mechanism appeared to be film diffusion controlled and data fitted best to Freundlich isotherm with regression value of 0.991. The discussion also focuses on few of the recently used adsorbents for Hg(II uptake and their comparison with the present study on the basis of removal percentage and kinetics involved

  4. Comparison of multifractal parameters form adsorption isotherms, desorption isotherms and mercury intrusion curves

    Science.gov (United States)

    Paz-Ferreiro, Jorge; Mon, Rodolfo; Vidal Vázquez, Eva

    2013-04-01

    The soil pore space is composed of a continuum of pores extremely variable in size, which range from equivalent diameter sizes smaller than nanometers to an upper limit of the order of centimeters. So, it is quite typical for soil pore space to display a size range of more than a factor of 106 in scale. Nitrogen sorption and mercury injection provide pores size distributions in the range from about 0.1 to 0.001 μm and 150 to 0.005 μm, respectively. The aims of this study were to evaluate the scaling properties of nitrogen adsorption isotherms (NAI), nitrogen desorption isotherms (NDI) and mercury intrusion porosimetry (MIP) curves of agricultural soils from "La Pampa húmeda", in the north of Buenos Aires and south of Santa Fé provinces, Argentina. Both NAIs, NDIs and MIPs exhibited multifractal behavior but its scaling properties were different so that the multifractality index, assessed by the width of the generalized dimension and the singularity spectra ranked as follows: NAI > NDI > MIP. Also, parameterization by the Hurst exponent indicates NAIs were less persistent than NDIs and in turn, these were less persistent than MIPs. The multfractal approach was useful to characterize the heterogeneity of various domains of the soil nano- micro- and mesopore system at the scale of small aggregates.

  5. Correlation and prediction of adsorption capacity and affinity of aromatic compounds on carbon nanotubes.

    Science.gov (United States)

    Wu, Wenhao; Yang, Kun; Chen, Wei; Wang, Wendi; Zhang, Jie; Lin, Daohui; Xing, Baoshan

    2016-01-01

    Adsorption of 22 nonpolar and polar aromatic compounds on 10 carbon nanotubes (CNTs) with various diameters, lengths and surface oxygen-containing group contents was investigated to develop predictive correlations for adsorption, using the isotherm fitting of Polanyi theory-based Dubinin-Ashtakhov (DA) model. Adsorption capacity of aromatic compounds on CNTs is negatively correlated with melting points of aromatic compounds, and surface oxygen-containing group contents and surface area ratios of mesopores to total pores of CNTs, but positively correlated with total surface area of CNTs. Adsorption affinity is positively correlated with solvatochromic parameters of aromatic compounds, independent of tube lengths and surface oxygen-containing group contents of CNTs, but negatively correlated with surface area ratios of mesopores to total pores of CNTs. The correlations of adsorption capacity and adsorption affinity with properties of both aromatic compounds and CNTs clearly have physical significance, can be used successfully with DA model to predict adsorption of aromatic compounds on CNTs from the well-known physiochemical properties of aromatic compounds (i.e., solvatochromic parameters, melting points) and CNTs (i.e., surface area and total acidic group contents), and thus can facilitate the environmental application of CNTs as sorbents and environmental risk assessment of both aromatic contaminants and CNTs.

  6. Carbon nanotube membranes with ultrahigh specific adsorption capacity for water desalination and purification.

    Science.gov (United States)

    Yang, Hui Ying; Han, Zhao Jun; Yu, Siu Fung; Pey, Kin Leong; Ostrikov, Kostya; Karnik, Rohit

    2013-01-01

    Development of technologies for water desalination and purification is critical to meet the global challenges of insufficient water supply and inadequate sanitation, especially for point-of-use applications. Conventional desalination methods are energy and operationally intensive, whereas adsorption-based techniques are simple and easy to use for point-of-use water purification, yet their capacity to remove salts is limited. Here we report that plasma-modified ultralong carbon nanotubes exhibit ultrahigh specific adsorption capacity for salt (exceeding 400% by weight) that is two orders of magnitude higher than that found in the current state-of-the-art activated carbon-based water treatment systems. We exploit this adsorption capacity in ultralong carbon nanotube-based membranes that can remove salt, as well as organic and metal contaminants. These ultralong carbon nanotube-based membranes may lead to next-generation rechargeable, point-of-use potable water purification appliances with superior desalination, disinfection and filtration properties. PMID:23941894

  7. Mercury

    Science.gov (United States)

    Mercury is an element that is found in air, water and soil. It has several forms. Metallic mercury is a shiny, silver-white, odorless liquid. If ... with other elements to form powders or crystals. Mercury is in many products. Metallic mercury is used ...

  8. Effects of temperature and volumetric loading rate on phenol adsorption capacity by granular activated carbon

    Directory of Open Access Journals (Sweden)

    Bamrungsri, P.

    2004-02-01

    Full Text Available The effects of temperature and volumetric loading rate on adsorption capacity of phenol by granular activated carbon were studied using F-300 and C2-115 granular activated carbon. All the experiments were conducted both in a batch study and a fixed-bed adsorption column study with the initial phenol concentration of 10 mg/l. In the batch study, the effects of temperature on the adsorption capacity and the rate of adsorption were determined. The results from the batch study showed that the rate of adsorption of F-300 was higher than that of C2-115. Moreover, it was clearly shown that the adsorption capacity increased with increasing temperature in both types of activated carbon at a contact time of 5 hours. In addition, the results from the fixed-bed column study revealed that the adsorption capacity decreased with increasing volumetric loading rate. Regression analysis expressed that the constants of Bohart-Adams Model ( K at volumetric loading rate of 2.5 , 5.0 and 10.0 m3/m2-hr were 0.0027 , 0.0063 and 0.0128 l/mg-hr for F-300 and 0.0021, 0.0071 and 0.0127 l/mg-hr for C2-115, respectively. N0 constant at volumetric loading rates of 2.5, 5.0 and 10.0 m3/ m2-hr were 30,393, 19,502 and 13,997 mg/l for F-300 and 27,752, 13,873 and 10,535 mg/l for C2-115, respectively. Thus, it can be summarized that the performance of F-300 was higher than that of C2-115 activated carbon at the studied conditions.

  9. Non-Contact Analysis of the Adsorptive Ink Capacity of Nano Silica Pigments on a Printing Coating Base

    Science.gov (United States)

    Jiang, Bo; Huang, Yu Dong

    2014-01-01

    Near infrared spectra combined with partial least squares were proposed as a means of non-contact analysis of the adsorptive ink capacity of recording coating materials in ink jet printing. First, the recording coating materials were prepared based on nano silica pigments. 80 samples of the recording coating materials were selected to develop the calibration of adsorptive ink capacity against ink adsorption (g/m2). The model developed predicted samples in the validation set with r2  = 0.80 and SEP  = 1.108, analytical results showed that near infrared spectra had significant potential for the adsorption of ink capacity on the recording coating. The influence of factors such as recording coating thickness, mass ratio silica: binder-polyvinyl alcohol and the solution concentration on the adsorptive ink capacity were studied. With the help of the near infrared spectra, the adsorptive ink capacity of a recording coating material can be rapidly controlled. PMID:25329464

  10. Polyhydroxyl-aluminum pillaring improved adsorption capacities of Pb2+ and Cd2+ onto diatomite

    Institute of Scientific and Technical Information of China (English)

    朱健; 王平; 雷明婧; 张伟丽

    2014-01-01

    In order to greatly improve adsorption capacity, the diatomite was pillared by polyhydroxyl-aluminum.A series of adsorption tests were conducted to obtain the optimum condition for pillared diatomite synthesis. The scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), surface area and porosity analyzer and micro-electrophoresis were used to determine pore structure and surface property.The pillared diatomite attaining the optimal adsorption densities (qe) of Pb2+ and Cd2+ was synthesized with the following conditions: Addition of pillaring solution containing Al3+-oligomers with a concentration range of 0.1-0.2 mol/L to a suspension containing Na+-diatomite to obtain the required Al/diatomite ratio of 10 mmol/g; synthesis temperature of 80 °C for 120 min; aging at a temperature of 105 °C for 16 h. The adsorption capacities of Pb2+ and Cd2+ on pillared diatomite increase by 23.79% and 27.36% compared with natural diatomite, respectively. The surface property of pillared diatomite is more favorable for ion adsorption than natural diatomite. The result suggests that diatomite can be modified by pillaring with polyhydroxyl-aluminum to improve its adsorption properties greatly.

  11. Facile preparation of hierarchical hollow structure gamma alumina and a study of its adsorption capacity

    Science.gov (United States)

    Lan, Shi; Guo, Na; Liu, Lu; Wu, Xiaomin; Li, Linlin; Gan, Shucai

    2013-10-01

    The hierarchical shell and hollow core structure gamma alumina (γ-Al2O3) with high adsorption affinity toward organic pollutants was fabricated via a facile homogeneous precipitation method. The microstructure, morphology, and functional groups of the as-synthesized γ-Al2O3 were characterized in detail. The N2 adsorption-desorption measurement (BET) experimental result showed the surface area of γ-Al2O3 (Al90-600) is 320.6 m2/g and the average pore size is 17.8 nm. The effects of reaction parameters on the synthesis of hierarchical hollow structure were systematically investigated. The dye removal ability of this adsorbent was determined by batch adsorption procedure. The isotherms and kinetics of adsorption process were determined and analyzed in detail, which were found to obey the Langmuir isotherm model and the pseudo-second-order for both the Congo red (CR) and Methyl orange (MO). The maximum adsorption capacity of γ-Al2O3 for CR is 835.0 mg/g, which is higher than that of many other previously reported hierarchical structured adsorbents. This facile synthetic approach is a very promising way for the design and synthesis of the typical hierarchical hollow structure materials with powerful adsorption capacity for the removal of organic contaminants from wastewater.

  12. Effect of purity on adsorption capacities of a Mars-like clay mineral at different pressures

    Science.gov (United States)

    Jenkins, Traci; Mcdoniel, Bridgett; Bustin, Roberta; Allton, Judith H.

    1992-01-01

    There has been considerable interest in adsorption of carbon dioxide on Marslike clay minerals. Some estimates of the carbon dioxide reservoir capacity of the martian regolith were calculated from the amount of carbon dioxide adsorbed on the ironrich smectite nontronite under martian conditions. The adsorption capacity of pure nontronite could place upper limits on the regolith carbon dioxide reservoir, both at present martian atmospheric pressure and at the postulated higher pressures required to permit liquid water on the surface. Adsorption of carbon dioxide on a Clay Mineral Society standard containing nontronite was studied over a wide range of pressures in the absence of water. Similar experiments were conducted on the pure nontronite extracted from the natural sample. Heating curves were obtained to help characterize and determine the purity of the clay sample.

  13. 3D hierarchical porous graphene aerogels for highly improved adsorption and recycled capacity

    Energy Technology Data Exchange (ETDEWEB)

    Chi, Caixia [School of Chemical Engineering and Technology, Harbin Institute of Technology, Xida Zhi street 92, Harbin 150001 (China); Food and Pharmaceutical Engineering College, Suihua University, Suihua 152061 (China); Xu, Hongbo [School of Chemical Engineering and Technology, Harbin Institute of Technology, Xida Zhi street 92, Harbin 150001 (China); Zhang, Ke, E-mail: zhangke@hit.edu.cn [School of Chemical Engineering and Technology, Harbin Institute of Technology, Xida Zhi street 92, Harbin 150001 (China); Wang, Yibo [School of Chemical Engineering and Technology, Harbin Institute of Technology, Xida Zhi street 92, Harbin 150001 (China); Zhang, Shuanghu [Food and Pharmaceutical Engineering College, Suihua University, Suihua 152061 (China); Liu, Xusong; Liu, Xin; Zhao, Jiupeng [School of Chemical Engineering and Technology, Harbin Institute of Technology, Xida Zhi street 92, Harbin 150001 (China); Li, Yao, E-mail: yaoli@hit.edu.cn [Center for Composite Materials, Harbin Institute of Technology, Harbin 150001 (China)

    2015-04-15

    Graphical abstract: - Highlights: • 3D HGAs were prepared by a “fishing” process. • Their porous morphologies were varied by changing of PS particles. • HGAs are used as adsorbents for removal of oils and organic solvents. • They exhibit highly improved adsorption and recycled capacity. - Abstract: This article demonstrates the fabrication of 3D hierarchical porous graphene aerogels (HGAs) with tunable porous architecture by a “fishing” process with polystyrene (PS) particles as sacrificial templates. Structure and morphology were characterized by X-ray diffraction (XRD), Raman spectroscopy, and scanning electron microscopy (SEM), respectively. The 3D HGAs exhibits low density, super hydrophobicity, high porosity and good thermal stability, which were used as adsorbents for removal of oils and organic solvents, showing highly efficient adsorption. In addition, they could be regenerated by heat treatment to release the adsorbates. After eight toluene-adsorbing and drying recycles, the adsorption capacity of HGAs reaches 93% of the initial uptake.

  14. Application of Epithermal Neutron Activation Analysis to Investigate Accumulation and Adsorption of Mercury by Spirulina platensis Biomass

    CERN Document Server

    Mosulishvili, L M; Khizanishvili, A I; Frontasyeva, M V; Kirkesali, E I; Aksenova, N G

    2004-01-01

    Epithermal neutron activation analysis was used to study interaction of blue-green alga Spirulina platensis with toxic metal mercury. Various concentrations of Hg(II) were added to cell cultures in a nutrient medium. The dynamics of accumulation of Hg was investigated over several days in relation to Spirulina biomass growth. The process of Hg adsorption by Spirulina biomass was studied in short-time experiments. The isotherm of adsorption was carried out in Freindlich coordinates. Natural Spirulina biomass has potential to be used in the remediation of sewage waters at Hg concentrations \\sim 100 {\\mu}g/l.

  15. Assessment of CO₂ adsorption capacity on activated carbons by a combination of batch and dynamic tests.

    Science.gov (United States)

    Balsamo, Marco; Silvestre-Albero, Ana; Silvestre-Albero, Joaquín; Erto, Alessandro; Rodríguez-Reinoso, Francisco; Lancia, Amedeo

    2014-05-27

    In this work, batch and dynamic adsorption tests are coupled for an accurate evaluation of CO2 adsorption performance of three different activated carbons (AC) obtained from olive stones by chemical activation followed by physical activation with CO2 at varying times (i.e., 20, 40, and 60 h). Kinetic and thermodynamic CO2 adsorption tests from simulated flue gas at different temperatures and CO2 pressures are carried out under both batch (a manometric equipment operating with pure CO2) and dynamic (a lab-scale fixed-bed column operating with a CO2/N2 mixture) conditions. The textural characterization of the AC samples shows a direct dependence of both micropore and ultramicropore volume on the activation time; hence, AC60 has the higher contribution. The adsorption tests conducted at 273 and 293 K showed that when CO2 pressure is lower than 0.3 bar, the lower the activation time, the higher CO2 adsorption capacity; a ranking of ω(eq)(AC20) > ω(eq)(AC40) > ω(eq)(AC60) can be exactly defined when T = 293 K. This result is likely ascribed to the narrower pore size distribution of the AC20 sample, whose smaller pores are more effective for CO2 capture at higher temperature and lower CO2 pressure, the latter representing operating conditions of major interest for decarbonation of flue gas effluent. Moreover, the experimental results obtained from dynamic tests confirm the results derived from the batch tests in terms of CO2 adsorption capacity. It is important to highlight the fact that the adsorption of N2 on the synthesized AC samples can be considered to be negligible. Finally, the importance of proper analysis for data characterization and adsorption experimental results is highlighted for the correct assessment of the CO2 removal performance of activated carbons at different CO2 pressures and operating temperatures. PMID:24784997

  16. Characteristics of fly ashes from full-scale coal-fired power plants and their relationship to mercury adsorption

    Science.gov (United States)

    Lu, Y.; Rostam-Abadi, M.; Chang, R.; Richardson, C.; Paradis, J.

    2007-01-01

    Nine fly ash samples were collected from the particulate collection devices (baghouse or electrostatic precipitator) of four full-scale pulverized coal (PC) utility boilers burning eastern bituminous coals (EB-PC ashes) and three cyclone utility boilers burning either Powder River Basin (PRB) coals or PRB blends,(PRB-CYC ashes). As-received fly ash samples were mechanically sieved to obtain six size fractions. Unburned carbon (UBC) content, mercury content, and Brunauer-Emmett-Teller (BET)-N2 surface areas of as-received fly ashes and their size fractions were measured. In addition, UBC particles were examined by scanning electron microscopy, high-resolution transmission microscopy, and thermogravimetry to obtain information on their surface morphology, structure, and oxidation reactivity. It was found that the UBC particles contained amorphous carbon, ribbon-shaped graphitic carbon, and highly ordered graphite structures. The mercury contents of the UBCs (Hg/UBC, in ppm) in raw ash samples were comparable to those of the UBC-enriched samples, indicating that mercury was mainly adsorbed on the UBC in fly ash. The UBC content decreased with a decreasing particle size range for all nine ashes. There was no correlation between the mercury and UBC contents of different size fractions of as-received ashes. The mercury content of the UBCs in each size fraction, however, generally increased with a decreasing particle size for the nine ashes. The mercury contents and surface areas of the UBCs in the PRB-CYC ashes were about 8 and 3 times higher than UBCs in the EB-PC ashes, respectively. It appeared that both the particle size and surface area of UBC could contribute to mercury capture. The particle size of the UBC in PRB-CYC ash and thus the external mass transfer was found to be the major factor impacting the mercury adsorption. Both the particle size and surface reactivity of the UBC in EB-PC ash, which generally had a lower carbon oxidation reactivity than the PRB

  17. Influence of the inherent properties of drinking water treatment residuals on their phosphorus adsorption capacities.

    Science.gov (United States)

    Bai, Leilei; Wang, Changhui; He, Liansheng; Pei, Yuansheng

    2014-12-01

    Batch experiments were conducted to investigate the phosphorus (P) adsorption and desorption on five drinking water treatment residuals (WTRs) collected from different regions in China. The physical and chemical characteristics of the five WTRs were determined. Combined with rotated principal component analysis, multiple regression analysis was used to analyze the relationship between the inherent properties of the WTRs and their P adsorption capacities. The results showed that the maximum P adsorption capacities of the five WTRs calculated using the Langmuir isotherm ranged from 4.17 to 8.20mg/g at a pH of 7 and further increased with a decrease in pH. The statistical analysis revealed that a factor related to Al and 200 mmol/L oxalate-extractable Al (Alox) accounted for 36.5% of the variations in the P adsorption. A similar portion (28.5%) was attributed to an integrated factor related to the pH, Fe, 200 mmol/L oxalate-extractable Fe (Feox), surface area and organic matter (OM) of the WTRs. However, factors related to other properties (Ca, P and 5 mmol/L oxalate-extractable Fe and Al) were rejected. In addition, the quantity of P desorption was limited and had a significant negative correlation with the (Feox+Alox) of the WTRs (p<0.05). Overall, WTRs with high contents of Alox, Feox and OM as well as large surface areas were proposed to be the best choice for P adsorption in practical applications.

  18. Effect of surface area and chemisorbed oxygen on the SO2 adsorption capacity of activated char

    Science.gov (United States)

    Lizzio, A.A.; DeBarr, J.A.

    1996-01-01

    The objective of this study was to determine whether activated char produced from Illinois coal could be used effectively to remove sulfur dioxide from coal combustion flue gas. Chars were prepared from a high-volatile Illinois bituminous coal under a wide range of pyrolysis and activation conditions. A novel char preparation technique was developed to prepare chars with SO2 adsorption capacities significantly greater than that of a commercial activated carbon. In general, there was no correlation between SO2 adsorption capacity and surface area. Temperature-programmed desorption (TPD) was used to determine the nature and extent of carbon-oxygen (C-O) complexes formed on the char surface. TPD data revealed that SO2 adsorption was inversely proportional to the amount of C-O complex. The formation of a stable C-O complex during char preparation may have served only to occupy carbon sites that were otherwise reactive towards SO2 adsorption. A fleeting C(O) complex formed during SO2 adsorption is postulated to be the reaction intermediate necessary for conversion of SO2 to H2SO4. Copyright ?? 1996 Elsevier Science Ltd.

  19. The Adsorption Capacity, Pore Structure, and Thermal Behavior of the Modified Clay Containing SSA

    Directory of Open Access Journals (Sweden)

    Haijun Lu

    2016-01-01

    Full Text Available Sewage sludge ash (SSA was created by burning municipal sludge. The potential of clay containing 1 or 3 or 5% SSA was assessed for use as a landfill liner-soil material. Batch adsorption, low temperature N2 adsorption, and TG-DTA tests were performed to evaluate the adsorption capacity, micropore structure, thermostability, and components of soils under Cr(VI and Pb(II chemical solutions. With the increasing amount of SSA in modified clay, the adsorption capacity of Cr(VI and Pb(II to the modified clay increases gradually. After absorption, the pore size of modified clay ranges from 2 nm to 8 nm. With the increasing amount of absorption, the pore volume decreases and the specific surface area increases. With the increasing of adsorption concentration of Cr(VI and Pb(II, the mass loss percentage of modified clay increases to 23.4% and 12.6%, respectively. The modified clay containing SSA may be used as a good barrier material to attenuate contamination of Cr(VI and Pb(II in landfills.

  20. Experimental and theoretical investigations of mercury adsorption on hematite (1-102) surfaces

    Science.gov (United States)

    Jung, J.; Wilcox, J.; Jew, A. D.; Rupp, E. C.; Brown, G. E.

    2013-12-01

    Fly ash is a primary byproduct of the coal combustion process. The release of fly ash into the environment and its use in consumer products are public health concerns because of the presence of toxic trace metals and metalloids, such as mercury (Hg), selenium (Se), and arsenic (As), which may exist as components of fly ash, partition onto fly ash as it cools, or is lost to the environment through smoke stacks in a vapor phase. Therefore, it is important to understand the components of fly ash and their interaction with trace metals. In this study, calculations using density functional theory (DFT) were carried out in conjunction with experimental studies to investigate the interaction between Hg and hematite, an important mineral component of fly ash. Our experimental study, designed to simulate Hg sorption in a coal-fired power plant exhaust system, involved exposure of the fine fraction of bituminous coal fly ash (≤ 0.1 μm) to methane combustion flue gas, supplemented with SO2, NOx, HCl, and Hg in a packed-bed reactor. Sorption reaction products were characterized by synchrotron-based x-ray fluorescence mapping (s-XRF), x-ray diffraction (XRD), and extended x-ray absorption fine structure (EXAFS) spectroscopy. Preliminary s-XRF results showed that Hg in the sample is correlated with Fe, S, Cl, Br, and to a lesser extent with Se and As. From the XRD analysis, the dominant mineral phases detected were quartz, iron oxide (hematite), and various sulfate-bearing cements. Based on the experimental results, DFT studies were carried out to investigate the adsorption of Hg on hematite (α-Fe2O3) (1-102) surfaces. The two α-Fe2O3 (1-102) surfaces modeled consisted of two different surface terminations: (1) M2-clean, which corresponds to the oxygen terminated r-cut surface with the first layer of cations removed and no hydroxyl group and (2) M2-OH2-OH which has bihydroxylated top oxygen atoms and a second layer of hydroxylated oxygen atoms. These surface terminations

  1. Mercury reduction and cell-surface adsorption by Geobacter sulfurreducens PCA

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Haiyan [ORNL; Lin, Hui [ORNL; Zheng, Wang [ORNL; Feng, Xinbin [ORNL; Liang, Liyuan [ORNL; Elias, Dwayne A [ORNL; Gu, Baohua [ORNL

    2013-01-01

    Both reduction and surface adsorption of mercuric mercury [Hg(II)] are found to occur simultaneously on G. sulfurreducens PCA cells under dark, anaerobic conditions. Reduction of Hg(II) to elemental Hg(0) initially follows a pseudo-first order kinetics with a half-life of < 2 h in the presence of 50 nM Hg(II) and 1011 cells L-1 in a phosphate buffer (pH 7.4). Multiple gene deletions of the outer membrane cytochromes in this organism resulted in decrease in reduction rate from ~ 0.3 to 0.05 h-1, and reduction was nearly absent with heat-killed cells or in the cell filtrate. Adsorption of Hg(II) by cells is found to compete with, and thus inhibit, Hg(II) reduction. Depending on the Hg to cell ratio, maximum Hg(II) reduction was observed at about 5 10-19 mol Hg cell-1, but reduction terminated at a low Hg to cell ratio (< 10-20 mol Hg cell-1). This inhibitory effect is attributed to strong binding between Hg(II) and the thiol ( SH) functional groups on cells and validated by experiments in which the sorbed Hg(II) was readily exchanged by thiols (e.g., glutathione) but not by carboxylic ligands such as ethylenediaminetetraacetate (EDTA). We suggest that coupled Hg(II)-cell interactions, i.e., reduction and surface binding, could be important in controlling Hg species transformation and bioavailability and should therefore be considered in microbial Hg(II) uptake and methylation studies.

  2. Enhanced formaldehyde-vapor adsorption capacity of polymeric amine-incorporated aminosilicas.

    Science.gov (United States)

    Nomura, Akihiro; Jones, Christopher W

    2014-05-19

    Airborne formaldehyde, which is a highly problematic volatile organic compound (VOC) pollutant, is adsorbed by polymeric amine-incorporated silicas (aminosilicas), and the factors that affect the adsorption performance are systematically investigated. Three different types of polymeric amines 1) poly(ethyleneimine) branched (PEIBR); 2) poly(ethyleneimine) linear (PEILI); and 3) poly(allylamine) (PAA) are impregnated into two types of porous silicas [SBA-15 and mesocellular foam (MCF) silicas] with systematic changes of the amine loadings. The adsorption results demonstrate that the adsorption capacity increases along with the amine loading until the polymeric amines completely fill the silica pores. This results in the MCF silica, which has a larger pore volume and hence can accommodate more polymeric amine before completely filling the pore, giving materials that adsorb more formaldehyde, with the largest adsorption capacity, q, of up to 5.7 mmolHCHO  g(-1) among the samples studied herein. Of the three different types of polymers, PAA, comprised of 100 % primary amines, showed the highest amine efficiency μ (mmolHCHO/mmolN) for capturing formaldehyde. The chemical structures of the adsorbed formaldehyde are analyzed by (13)C cross-polarization magic-angle spinning (CP-MAS) NMR, and it is demonstrated that the adsorbed formaldehyde is chemically attached to the aminosilica surface, forming hemiaminal and imine species. Because the chemical adsorption of formaldehyde forms covalent bonds, it is not desorbed from the aminosilicas below 130 °C based on temperature-programed-desorption (TPD) analysis. The high formaldehyde-adsorption capacity and stability of the trapped formaldehyde on the amine surface in this study reveal the potential utility of aminosilicas as formaldehyde abatement materials.

  3. Powder-based adsorbents having high adsorption capacities for recovering dissolved metals and methods thereof

    Science.gov (United States)

    Janke, Christopher J.; Dai, Sheng; Oyola, Yatsandra

    2016-05-03

    A powder-based adsorbent and a related method of manufacture are provided. The powder-based adsorbent includes polymer powder with grafted side chains and an increased surface area per unit weight to increase the adsorption of dissolved metals, for example uranium, from aqueous solutions. A method for forming the powder-based adsorbent includes irradiating polymer powder, grafting with polymerizable reactive monomers, reacting with hydroxylamine, and conditioning with an alkaline solution. Powder-based adsorbents formed according to the present method demonstrated a significantly improved uranium adsorption capacity per unit weight over existing adsorbents.

  4. Novel biosorbent with high adsorption capacity prepared by chemical modification of white pine (Pinus durangensis) sawdust. Adsorption of Pb(II) from aqueous solutions.

    Science.gov (United States)

    Salazar-Rabago, J J; Leyva-Ramos, R

    2016-03-15

    The natural sawdust (NS) from white pine (Pinus durangensis) was chemically modified by a hydrothermal procedure using citric, malonic and tartaric acids. The adsorption capacity of modified sawdust (MS) towards Pb(II) was considerably enhanced due to the introduction of carboxylic groups on the surface of MS during the modification, and the adsorption capacity was almost linearly dependent on the concentration of carboxylic sites. The NS surface was acidic, and the MS surface became more acidic after the modification. At T = 25 °C and pH = 5, the maximum adsorption capacity of the optimal MS towards Pb(II) was 304 mg/g, which is exceptionally high compared to NS and other MS reported previously. The adsorption capacity of MS was considerably reduced from 304 to 154 mg/g by decreasing the solution pH from 5 to 3 due to electrostatic interactions. The adsorption of Pb(II) on MS was reversible at pH = 2, but not at pH = 5. The contribution percentage of ion exchange to the overall adsorption capacity ranged from 70 to 99% and 10-66% at the initial pH of 3 and 5, respectively. Hence, the adsorption of Pb(II) on MS was mainly due to ion exchange at pH = 3 and to both ion exchange and electrostatic attraction at pH = 5.

  5. Adsorptive behaviour of mercury on algal biomass: Competition with divalent cations and organic compounds

    Energy Technology Data Exchange (ETDEWEB)

    Carro, Leticia; Barriada, Jose L. [Departamento de Quimica Fisica e Ingenieria Quimica I, Universidad de A Coruna, c/Rua da Fraga 10, 15008 A Coruna (Spain); Herrero, Roberto, E-mail: r.herrero@udc.es [Departamento de Quimica Fisica e Ingenieria Quimica I, Universidad de A Coruna, c/Rua da Fraga 10, 15008 A Coruna (Spain); Sastre de Vicente, Manuel E. [Departamento de Quimica Fisica e Ingenieria Quimica I, Universidad de A Coruna, c/Rua da Fraga 10, 15008 A Coruna (Spain)

    2011-08-15

    Highlights: {yields} Native and protonated macroalga S. muticum are good materials for mercury removal. {yields} Fast kinetic process and high mercury uptakes have been found for those materials. {yields} Diffusion control is the rate limiting step of the process. {yields} Competition effects by organic compounds, inorganic salts and divalent cations were analyzed. {yields} Continuous flow experiments allowed identification of mercury reduction during metal removal. - Abstract: Biosorption processes constitute an effective technique for mercury elimination. Sorption properties of native and acid-treated Sargassum muticum have been studied. Effect of pH, initial mercury concentration and contact time studies provided fundamental information about the sorption process. This information was used as the reference values to analyse mercury sorption under competition conditions. Saline effect has shown little influence in sorption, when only electrostatic modifications took place upon salt addition. On the contrary, if mercury speciation dramatically changed owing to the addition of an electrolyte, such as in the case of chloride salt, very large modifications in mercury sorption were observed. Competition with other divalent cations or organic compounds has shown little or none effect on mercury, indicating that a different mechanism is taking place during the removal of these pollutants. Finally, continuous flow experiments have clearly shown that a reduction process is also taking place during mercury removal. This fact is not obvious to elucidate under batch sorption experiments. Scanning Electron Microscopy analysis of the surface of the materials show deposits of mercury(I) and metallic mercury which is indicative of the reduction process proposed.

  6. Effect of surface modification of activated carbon on its adsorption capacity for NH3

    Institute of Scientific and Technical Information of China (English)

    SHAN Xiao-mei; ZHU Shu-quan; ZHANG Wen-hui

    2008-01-01

    To investigate the effects of carbon surface characteristics on NH3 adsorption, coal-based and coconut shell activated carbons were modified by treatment with oxidants. The surface properties of the carbons were characterized by low temperature nitrogen sorption, by Boehm's titrations and by XPS techniques. NH3 adsorption isotherms of the original and the modified carbons were determined. The results show that the carbons were oxidized by HNO3 and (NH4)2S2O8, and that there was an increase in oxygen containing functional groups on the surface. However, the pore-size distribution of the coal-based carbons was changed after KMnO4 treatment. It was found that the NH3 adsorption capacity of the modified carbons was enhanced and that the most pronounced enhancement results from (NH4)2S2O8 oxidation. Under our experimental conditions, the capacity is positively corrected to the number of surface functional groups containing oxygen, and to the number of micro-pores. Furthermore, an empirical model of the relationship between NH3 adsorption and multiple factors on the carbon surface was fit using a complex regression method.

  7. Comparative study of carbon nanotubes and granular activated carbon: Physicochemical properties and adsorption capacities.

    Science.gov (United States)

    Gangupomu, Roja Haritha; Sattler, Melanie L; Ramirez, David

    2016-01-25

    The overall goal was to determine an optimum pre-treatment condition for carbon nanotubes (CNTs) to facilitate air pollutant adsorption. Various combinations of heat and chemical pre-treatment were explored, and toluene was tested as an example hazardous air pollutant adsorbate. Specific objectives were (1) to characterize raw and pre-treated single-wall (SW) and multi-wall (MW) CNTs and compare their physical/chemical properties to commercially available granular activated carbon (GAC), (2) to determine the adsorption capacities for toluene onto pre-treated CNTs vs. GAC. CNTs were purified via heat-treatment at 400 °C in steam, followed by nitric acid treatment (3N, 5N, 11N, 16N) for 3-12 h to create openings to facilitate adsorption onto interior CNT sites. For SWNT, Raman spectroscopy showed that acid treatment removed impurities up to a point, but amorphous carbon reformed with 10h-6N acid treatment. Surface area of SWNTs with 3 h-3N acid treatment (1347 m(2)/g) was higher than the raw sample (1136 m(2)/g), and their toluene maximum adsorption capacity was comparable to GAC. When bed effluent reached 10% of inlet concentration (breakthrough indicating time for bed cleaning), SWNTs had adsorbed 240 mg/g of toluene, compared to 150 mg/g for GAC. Physical/chemical analyses showed no substantial difference for pre-treated vs. raw MWNTs. PMID:26476807

  8. Examination of zinc adsorption capacity of soils treated with different pyrolysis products

    Directory of Open Access Journals (Sweden)

    Rétháti Gabriella

    2014-11-01

    Full Text Available Organic matter input into soils is essential regarding agricultural, environmental and soil science aspects as well. However, the application of the pyrolysed forms of biochars and materials with different organic matter content gained more attention in order to decrease the emission of the green house gases (CO2, N2O from the soil. During pyrolysis, the materials containing high organic matter (biomass-originated organic matter are heated in oxygen-free (or limited amount of oxygen environment. As a result, the solid phase, which remains after eliminating the gases and liquid phase, is more stable compared to the original product, it cannot be mineralized easily in the soil and its utilization is more beneficial in terms of climatic aspects. Furthermore, it can improve soil structure and it can retain soil moisture and cations in the topsoil for long periods of time, which is very important for plants. In our experiment, the effects of biochar and bone char were examined on soils by zinc adsorption experiments. Based on our experiments, we concluded that the pyrolysis products can have significant Zn adsorption capacity compared to the soil. Bone ash can adsorb more Zn than the charcoal product. The Zn adsorption capacity of soils treated by pyrolysis products can be described by Langmuir adsorption isotherms. However, based on the amount of pyrolysis products, one or two term Langmuir isotherm fits well on the experiment data, which depends on the time the pyrolysis product has spent in the soil.

  9. A Porous Aromatic Framework Constructed from Benzene Rings Has a High Adsorption Capacity for Perfluorooctane Sulfonate

    Science.gov (United States)

    Luo, Qin; Zhao, Changwei; Liu, Guixia; Ren, Hao

    2016-02-01

    A low-cost and easily constructed porous aromatic framework (PAF-45) was successfully prepared using the Scholl reaction. PAF-45 was, for the first time, used to remove perfluorooctane sulfonate (PFOS) from aqueous solution. Systematic experiments were performed to determine the adsorption capacity of PAF-45 for PFOS and to characterize the kinetics of the adsorption process. The adsorption of PFOS onto PAF-45 reached equilibrium in 30 min, and the adsorption capacity of PAF-45 for PFOS was excellent (5847 mg g-1 at pH 3). The amount of PFOS adsorbed by PAF-45 increased significantly as the cation (Na+, Mg2+, or Fe3+) concentration increased, which probably occurred because the cations enhanced the interactions between the negatively charged PFOS molecules and the positively charged PAF-45 surface. The cations Na+, Mg2+, and Fe3+ were found to form complexes with PFOS anions in solution. Density functional theory was used to identify the interactions between PFOS and Na+, Mg2+, and Fe3+. We expect that materials of the same type as PAF-45 could be useful adsorbents for removing organic pollutants from industrial wastewater and contaminated surface water.

  10. Dispersion of chitosan on perlite for enhancement of copper(II) adsorption capacity.

    Science.gov (United States)

    Hasan, Shameem; Ghosh, Tushar K; Viswanath, Dabir S; Boddu, Veera M

    2008-04-01

    Chitosan coated perlite beads were prepared by drop-wise addition of slurry, made of chitosan dissolved in oxalic acid and perlite, to an alkaline bath (0.7 M NaOH). The beads that contained 32% chitosan enhanced the accessibility of OH and amine groups present in chitosan for adsorption of copper ions. The experiments using Cu(II) ions were carried out in the concentration range of 50-4100 mg/L (0.78-64.1 mmol/L). Adsorption capacity for Cu(II) was pH dependent and a maximum uptake of 104 mg/g of beads (325 mg/g of chitosan) was obtained at pH 4.5 when its equilibrium concentration in the solution was 812.5 mg/L at 298 K. The XPS and TEM data suggested that copper was mainly adsorbed as Cu(II) and was attached to amine groups. The adsorption data could be fitted to one-site Langmuir adsorption model. Anions in the solution had minimal effect on Cu(II) adsorption by chitosan coated perlite beads. EDTA was used effectively for the regeneration of the bed. The diffusion coefficient of Cu(II) onto chitosan coated beads was calculated from the breakthrough curve and was found to be 2.02 x 10(-8) cm(2)/s.

  11. Adsorption capacity of methylene blue, an organic pollutant, by montmorillonite clay

    KAUST Repository

    Feddal, I.

    2013-11-19

    The isotherms and kinetics of the adsorption of a cationic dye in aqueous solution, methylene blue, on a local Algerian montmorillonite clay mineral (raw, sodium and thermally activated at 300 and 500°C) were determined experimentally. Various parameters influencing the adsorption were optimized, mainly solid-liquid contact time, mass of adsorbent, initial concentration of dye, pH of the solution and temperature. Results showed that the adsorption kinetics were fast: 30 min for the raw clay mineral, and 20 min for sodium clay mineral (SC) and thermally activated at 300°C, whereas with the clay mineral calcined at 500°C, the equilibrium was reached after 150 min only. The maximum adsorption capacity was reached at pH 6.6. Results deducted from the adsorption isotherms also showed that the retention follows the Langmuir model. In addition, it was found that the kinetics were in the order of 2 (K = 2.457 × 106 g/mg.h) for sodium clay and were limited by an intra-particle diffusion. SC was found to be a better adsorbent to remove methylene blue from industrial wastewater. © 2013 Balaban Desalination Publications. All rights reserved.

  12. Simulation of Gaseous Mercury Adsorption of Different Building Materials%不同建筑材料对气态汞的吸附模拟研究

    Institute of Scientific and Technical Information of China (English)

    高小峰; 谷依露; 谢田; 刘阳; 黄晟; 赵由才

    2014-01-01

    The mechanical properties ,phase change energy storage ,environmental protection ,and recycling of building materials are extensively studied ,but few studies focus on the mercury adsorption of different building materials .Five types of cement brick pow der including foam concrete ,red brick ,aggregate and gravel as well as several standard concrete blocks were exposed to gaseous mercury in constant temperature to determine most vulnerable building material to mercury contamination and the contamination depth of concrete blocks .Results showed that small particle contributed to large mercury adsorption , however different performance was found amongvarious materials . Red brick was the likely to have strong adsorption capacity followed by foam concrete and gravel . For concrete block ,the pollution mainly concentratedat the 0~1.5cm of the surface .As a result ,for some seriously mercury polluted factories and workshops ,mercury pollution can be removed by peeling the skin of the buildings before demolition , renovation process .%建筑材料的力学性质、相变蓄能、生态环保、再生利用等受到广泛关注,但很少有关于不同建筑材料对汞的吸附研究。通过对水泥砖、泡沫混凝土、红砖、骨料、砂石等5种建筑材料细粉和水泥混凝土立方体标准试块置于恒温室内进行气态汞吸附模拟,探索出最易受汞污染的建筑材料和水泥混凝土块的受污染深度。通过XRD和XRF对5种建筑材料分析得出其成分以SiO2为主,其次是CaCO3。5种建筑材料进行汞吸附实验结果表明,整体上粒径越小吸附量越大,但不同材料之间存在差异性,红砖是最容易受污染的建筑材料,其次泡沫混凝土和砂石对汞也具有较大吸附性,水泥砖和骨料对汞吸附能力较弱。水泥混凝土块吸附模拟表明污染主要存在于表层0~1.5 cm范围内,汞污染严重的工厂和车间等在拆迁、改建过程中,需要对其表层剥离,去除汞污染。

  13. Influence of the inherent properties of drinking water treatment residuals on their phosphorus adsorption capacities

    Institute of Scientific and Technical Information of China (English)

    Leilei Bai; Changhui Wang; Liansheng He; Yuansheng Pei

    2014-01-01

    Batch experiments were conducted to investigate the phosphorus (P) adsorption and desorption on five drinking water treatment residuals (WTRs) collected from different regions in China.The physical and chemical characteristics of the five WTRs were determined.Combined with rotated principal component analysis,multiple regression analysis was used to analyze the relationship between the inherent properties of the WTRs and their P adsorption capacities.The results showed that the maximum P adsorption capacities of the five WTRs calculated using the Langmuir isotherm ranged from 4.17 to 8.20 mg/g at a pH of 7 and further increased with a decrease in pH.The statistical analysis revealed that a factor related to Al and 200 mmol/L oxalate-extractable Al (Alox) accounted for 36.5% of the variations in the P adsorption.A similar portion (28.5%) was attributed to an integrated factor related to the pH,Fe,200 mmol/L oxalate-extractable Fe (Feox),surface area and organic matter (OM) of the WTRs.However,factors related to other properties (Ca,P and 5 mmol/L oxalate-extractable Fe and Al) were rejected.In addition,the quantity of P desorption was limited and had a significant negative correlation with the (Feox + Alox) of the WTRs (p < 0.05).Overall,WTRs with high contents of Alox,Feox and OM as well as large surface areas were proposed to be the best choice for P adsorption in practical applications.

  14. Oil Spill Adsorption Capacity of Activated Carbon Tablets from Corncobs in Simulated Oil-Water Mixture

    Directory of Open Access Journals (Sweden)

    Rhonalyn V. Maulion

    2015-12-01

    Full Text Available Oil spill in bodies of water is one of severe environmental problems that is facing all over the country and in the world. Since oil is an integral part of the economy, increasing trend for its demand and transport of has led to a great treat in the surface water. One of the promising techniques in the removal of the oil spills in water bodies is adsorption using activated carbon form waste material such as corn cobs. The purpose of this study is to determine the adsorption capacity of activated carbon tablets derived from corncobs in the removal of oil. The properties of activated carbon produced have a pH of 7.0, bulk density of 0.26 g//cm3 , average pore size of 45nm, particle size of 18% at 60 mesh and 39% at 80 mesh, iodine number of 1370 mg/g and surface area of 1205 g/m2. The amount of bentonite clay as binder (15%,20%,30%, number of ACT (1,2,3 and time of contact(30,60,90 mins has been varied to determine the optimum condition where the activated carbon will have the best adsorption capacity in the removal of oil. Results showed that at 15% binder, 60 mins contact time and 3 tablets of activated carbon is the optimum condition which give a percentage adsorption of 22.82% of oil. Experimental data also showed that a Langmuir isotherm was the best fit isotherm for adsorption of ACT.

  15. New method for the preparation of adsorbent with high adsorption capacity

    Institute of Scientific and Technical Information of China (English)

    WANG Yongjian; LIU Jianfeng; DUO Jia; YU Yaoting

    2005-01-01

    Polyamidoamine (PAMAM) is a type of macro- molecule having a definite chemical structure and a large number of terminal functional groups. The synthetic approach of the adsorbent with high adsorption capacity involved arching of PAMAM onto cellulose beads by reaction with epichlorohydrin. The product thus prepared had a large number of amino groups of 2.94 mmol/g derived from 0.23 mmol/g epoxy groups on cellulose beads. This method presents an effective method for the preparation of high-loading adsorbents.

  16. ADSORPTION CAPACITY OF ACTIVATED CARBON FIBER FABRIC IN CYANIDE LEACHING LIQUOR OF GOLD ORES

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Adsorption capacity of ACFF in cyanide leaching liquor of gold ores was studied withcyanide leaching liquor of gold ores, containing various kinds of ions. The adsorbed leaching liquorwas analyzed by atomic emission spectroscopy and colorimetric method. The contents of variouskinds of ions in ACFF were determined with X-ray photoctron spectroscopy. ACFF not onlyadsorbed gold but also adsorbed arsenic, nickel, zinc, calcium, sulphur, bismuth, copper, iron. silverand cyanide anion. Atomic percentage of C and those of O, N, Zr, Fe increase and decreaserespectively with the increase of the layer depth, while those of Ca, Au, Ag keep constant.

  17. Intra- and inter-unit variation in fly ash petrography and mercury adsorption: Examples from a western Kentucky power station

    Science.gov (United States)

    Hower, J.C.; Finkelman, R.B.; Rathbone, R.F.; Goodman, J.

    2000-01-01

    Fly ash was collected from eight mechanical and 10 baghouse hoppers at each of the twin 150-MW wall-fired units in a western Kentucky power station. The fuel burned at that time was a blend of many low-sulfur, high-volatile bituminous Central Appalachian coals. The baghouse ash showed less variation between units than the mechanical hoppers. The mechanical fly ash, coarser than the baghouse ash, showed significant differences in the amount of total carbon and in the ratio of isotropic coke to both total carbon and total coke - the latter excluding inertinite and other unburned, uncoked coal. There was no significant variation in proportions of inorganic fly ash constituents. The inter-unit differences in the amount and forms of mechanical fly ash carbon appear to be related to differences in pulverizer efficiency, leading to greater amounts of coarse coal, therefore unburned carbon, in one of the units. Mercury capture is a function of both the total carbon content and the gas temperature at the point of fly ash separation, mercury content increasing with an increase in carbon for a specific collection system. Mercury adsorption on fly ash carbon increases at lower flue-gas temperatures. Baghouse fly ash, collected at a lower temperature than the higher-carbon mechanically separated fly ash, contains a significantly greater amount of Hg.

  18. Adsorption capacities of activated carbons for geosmin and 2-methylisoborneol vary with activated carbon particle size: Effects of adsorbent and adsorbate characteristics.

    Science.gov (United States)

    Matsui, Yoshihiko; Nakao, Soichi; Sakamoto, Asuka; Taniguchi, Takuma; Pan, Long; Matsushita, Taku; Shirasaki, Nobutaka

    2015-11-15

    The adsorption capacities of nine activated carbons for geosmin and 2-methylisoborneol (MIB) were evaluated. For some carbons, adsorption capacity substantially increased when carbon particle diameter was decreased from a few tens of micrometers to a few micrometers, whereas for other carbons, the increase of adsorption capacity was small for MIB and moderate for geosmin. An increase of adsorption capacity was observed for other hydrophobic adsorbates besides geosmin and MIB, but not for hydrophilic adsorbates. The parameter values of a shell adsorption model describing the increase of adsorption capacity were negatively correlated with the oxygen content of the carbon among other characteristics. Low oxygen content indicated low hydrophilicity. The increase of adsorption capacity was related to the hydrophobic properties of both adsorbates and activated carbons. For adsorptive removal of hydrophobic micropollutants such as geosmin, it is therefore recommended that less-hydrophilic activated carbons, such as coconut-shell-based carbons, be microground to a particle diameter of a few micrometers to enhance their equilibrium adsorption capacity. In contrast, adsorption by hydrophilic carbons or adsorption of hydrophilic adsorbates occur in the inner pores, and therefore adsorption capacity is unchanged by particle size reduction. PMID:26302219

  19. Adsorption capacities of activated carbons for geosmin and 2-methylisoborneol vary with activated carbon particle size: Effects of adsorbent and adsorbate characteristics.

    Science.gov (United States)

    Matsui, Yoshihiko; Nakao, Soichi; Sakamoto, Asuka; Taniguchi, Takuma; Pan, Long; Matsushita, Taku; Shirasaki, Nobutaka

    2015-11-15

    The adsorption capacities of nine activated carbons for geosmin and 2-methylisoborneol (MIB) were evaluated. For some carbons, adsorption capacity substantially increased when carbon particle diameter was decreased from a few tens of micrometers to a few micrometers, whereas for other carbons, the increase of adsorption capacity was small for MIB and moderate for geosmin. An increase of adsorption capacity was observed for other hydrophobic adsorbates besides geosmin and MIB, but not for hydrophilic adsorbates. The parameter values of a shell adsorption model describing the increase of adsorption capacity were negatively correlated with the oxygen content of the carbon among other characteristics. Low oxygen content indicated low hydrophilicity. The increase of adsorption capacity was related to the hydrophobic properties of both adsorbates and activated carbons. For adsorptive removal of hydrophobic micropollutants such as geosmin, it is therefore recommended that less-hydrophilic activated carbons, such as coconut-shell-based carbons, be microground to a particle diameter of a few micrometers to enhance their equilibrium adsorption capacity. In contrast, adsorption by hydrophilic carbons or adsorption of hydrophilic adsorbates occur in the inner pores, and therefore adsorption capacity is unchanged by particle size reduction.

  20. Synthesis and Characterization of Al-Cr-Pillared Montmorillonite with High Thermal Stability and Adsorption Capacity

    Institute of Scientific and Technical Information of China (English)

    CAO Ming-li; LIU Shi-zhen; YU Yong-fu

    2004-01-01

    Al-Cr-pillared montmorillonite was synthesized by using bentonite and Al-Cr pillaring solutionsas starting materials. The basal spacing and specific surface areas of the materials were significantly increased rela-tive to those of untreated clays. When the Al/Cr molar ratio ( R ) was 0.10, the d (001) value and specific surfacearea of pillared montmorillonite were 1.9194 nm and 165.7 m2 g- 1 , respectively. Thermal stability of the mate-rials was determined using calcined tests and X- ray diffraction (XRD) analysis. The materials formed at differentR(0.05;0.10;0.15;0.25) exhibit a high thermal stability at 300℃ , especially at initial R = 0.10, the basalinterlayer spacing of materials is stabilized at 1.7313 nm after calcined at 500℃ for 2 h. Adsorption behavior ofthe materials was studied by adsorption experiments. The results show that the Al- Cr-pillared montmorillonites ex-hibit much stronger adsorption capacity on Cr6+ in aqueous solution than untreated clays do.

  1. Diamine-appended metal-organic frameworks: enhanced formaldehyde-vapor adsorption capacity, superior recyclability and water resistibility.

    Science.gov (United States)

    Wang, Zhong; Wang, WenZhong; Jiang, Dong; Zhang, Ling; Zheng, Yali

    2016-07-28

    Capturing formaldehyde (HCHO) from indoor air with porous adsorbents still faces challenges due to their low uptake capacity, difficult regeneration, and especially, the sorption capacity reduction that is caused by the competitive adsorption of H2O when exposed to a humid atmosphere. In this work, MIL-101 is modified with ethylenediamine (ED) on its open-metal sites to substantially improve the HCHO adsorption properties. The HCHO uptake capacity of modified MIL-101 can be up to 5.49 mmol g(-1) in this study, which is among the highest-levels of various adsorbents reported thus far. Moreover, this modification both improved the material's recyclability and water resistibility, allowing for cyclic and selective tests with stable adsorption capacities, revealing the potential utility of amine-modified MOFs for indoor air purification. PMID:27338802

  2. Diamine-appended metal-organic frameworks: enhanced formaldehyde-vapor adsorption capacity, superior recyclability and water resistibility.

    Science.gov (United States)

    Wang, Zhong; Wang, WenZhong; Jiang, Dong; Zhang, Ling; Zheng, Yali

    2016-07-28

    Capturing formaldehyde (HCHO) from indoor air with porous adsorbents still faces challenges due to their low uptake capacity, difficult regeneration, and especially, the sorption capacity reduction that is caused by the competitive adsorption of H2O when exposed to a humid atmosphere. In this work, MIL-101 is modified with ethylenediamine (ED) on its open-metal sites to substantially improve the HCHO adsorption properties. The HCHO uptake capacity of modified MIL-101 can be up to 5.49 mmol g(-1) in this study, which is among the highest-levels of various adsorbents reported thus far. Moreover, this modification both improved the material's recyclability and water resistibility, allowing for cyclic and selective tests with stable adsorption capacities, revealing the potential utility of amine-modified MOFs for indoor air purification.

  3. Ultra-high adsorption capacity of zeolitic imidazole framework-67 (ZIF-67) for removal of malachite green from water.

    Science.gov (United States)

    Lin, Kun-Yi Andrew; Chang, Hsuan-Ang

    2015-11-01

    Zeolitic imidazole frameworks (ZIFs), a new class of adsorbents, are proposed to adsorb Malachite Green (MG) in water. Particularly, ZIF-67 was selected owing to its stability in water and straightforward synthesis. The as-synthesized ZIF-67 was characterized and used to adsorb MG from water. Factors affecting the adsorption capacity were investigated including mixing time, temperature, the presence of salts and pH. The kinetics, adsorption isotherm and thermodynamics of the MG adsorption to ZIF-67 were also studied. The adsorption capacity of ZIF-67 for MG could be as high as 2430mgg(-1) at 20°C, which could be improved at the higher temperatures. Such an ultra-high adsorption capacity of ZIF-67 was almost 10-times of those of conventional adsorbents, including activated carbons and biopolymers. A mechanism for the high adsorption capacity was proposed and possibly attributed to the π-π stacking interaction between MG and ZIF-67. ZIF-67 also could be conveniently regenerated by washing with ethanol and the regeneration efficiency could remain 95% up to 4 cycles of the regeneration. ZIF-67 was also able to remove MG from the aquaculture wastewater, in which MG can be typically found. These features enable ZIF-67 to be one of the most effective and promising adsorbent to remove MG from water.

  4. Study on the Adsorption Capacities for Airborne Particulates of Landscape Plants in Different Polluted Regions in Beijing (China

    Directory of Open Access Journals (Sweden)

    Wei-Kang Zhang

    2015-08-01

    Full Text Available Urban landscape plants are an important component of the urban ecosystem, playing a significant role in the adsorption of airborne particulates and air purification. In this study, six common landscape plants in Beijing were chosen as research subjects, and the adsorption capacities for each different plant leaf and the effects of the leaf structures for the adsorption capacities for particulates were determined. Preliminary results show that needle-leaved tree species adsorbed more airborne particulates than broad-leaved tree species for the same leaf area. Pinus tabuliformis exhibits the highest adsorption capacity, at 3.89 ± 0.026 μg·cm−2, almost two times as much as that of Populus tomentosa (2.00 ± 0.118 μg·cm−2. The adsorption capacities for PM10 of the same tree species leaves, in different polluted regions had significant differences, and the adsorption capacities for PM10 of the tree species leaf beside the Fifth Ring Road were higher than those of the tree species leaves in the Botanical Garden, although the adsorption capacities for PM2.5 of the same tree species in different polluted regions had no significant differences. By determining the soluble ion concentrations of the airborne particulates in two regions, it is suggested that the soluble ion concentrations of PM10 in the atmosphere in the Botanical Garden and beside the Fifth Ring Road have significant differences, while those of PM2.5 in the atmosphere had no significant differences. In different polluted regions there are significant adaptive changes to the leaf structures, and when compared with slightly polluted region, in the seriously polluted region the epidermis cells of the plant leaves shrinked, the surface textures of the leaves became rougher, and the stomas’ frequency and the pubescence length increased. Even though the plant leaves exposed to the seriously polluted region changed significantly, these plants can still grow normally and healthily.

  5. Reservoir capacity estimates in shale plays based on experimental adsorption data

    Science.gov (United States)

    Ngo, Tan

    from different measurement techniques using representative fluids (such as CH4 and CO2) at elevated pressures, and the adsorbed density can range anywhere between the liquid and the solid state of the adsorbate. Whether these discrepancies are associated with the inherent heterogeneity of mudrocks and/or with poor data quality requires more experiments under well-controlled conditions. Nevertheless, it has been found in this study that methane GIP estimates can vary between 10-45% and 10-30%, respectively, depending on whether the free or the total amount of gas is considered. Accordingly, CO2 storage estimates range between 30-90% and 15-50%, due to the larger adsorption capacity and gas density at similar pressure and temperature conditions. A manometric system has been designed and built that allows measuring the adsorption of supercritical fluids in microporous materials. Preliminary adsorption tests have been performed using a microporous 13X zeolite and CO 2 as an adsorbing gas at a temperature of 25oC and 35oC and at pressures up to 500 psi. Under these conditions, adsorption is quantified with a precision of +/- 3%. However, relative differences up to 15-20% have been observed with respect to data published in the literature on the same adsorbent and at similar experimental conditions. While it cannot be fully explained with uncertainty analysis, this discrepancy can be reduced by improving experiment practice, thus including the application of a higher adsorbent's regeneration temperature, of longer equilibrium times and of a careful flushing of the system between the various experimental steps. Based on the results on 13X zeolite, virtual tests have been conducted to predict the performance of the manometric system to measure adsorption on less adsorbing materials, such as mudrocks. The results show that uncertainties in the estimated adsorbed amount are much more significant in shale material and they increase with increasing pressure. In fact, relative

  6. The effect of food and ice cream on the adsorption capacity of paracetamol to high surface activated charcoal

    DEFF Research Database (Denmark)

    Høgberg, Lotte Christine Groth; Angelo, Helle Riis; Christophersen, Anne Bolette;

    2003-01-01

    The effect of added food mixture (as if food was present in the stomach of an intoxicated patient) or 4 different types of ice cream (added as a flavouring and lubricating agent) on the adsorption of paracetamol (acetaminophen) to 2 formulations of activated charcoal was determined in vitro......, and paracetamol were mixed with either food mixture or ice cream followed by one hr incubation. The maximum adsorption capacity of paracetamol to activated charcoal was calculated using Langmuirs adsorption isotherm. Paracetamol concentration was analyzed using high pressure liquid chromatography. In the presence...... of food, the paracetamol adsorption capacity of the 2 activated charcoals was reduced by max. 19% (Pfood (Hoegberg et al. 2002). Depending on which type of ice cream was mixed with the charcoal...

  7. Adsorption capacity of hydrophobic SiO2 aerogel/activated carbon composite materials for TNT

    Institute of Scientific and Technical Information of China (English)

    ZHOU; XiaoFang; CUI; Sheng; LIU; Yu; LIU; XueYong; SHEN; XiaoDong; WU; ZhanWu

    2013-01-01

    The adsorption properties of TNT from wastewater by hydrophobic silica aerogel/activated carbon composite materials were investigated. The effects of adsorption time, pH value, adsorption temperature, and the amount of the composite materials on the adsorption rate were studied. The adsorption principle and mechanism of the composite materials were discussed along with the Freundlich equation. The results showed that the best adsorption rate of the hydrophobic silica aerogel/activated car-bon composite materials could reach 96.5% with adsorption conditions of adsorption temperature 25°C, pH value 7, the amount of SiO2aerogel dosage 3.33 g/L, and adsorption time of 120 min. The adsorption of hydrophobic SiO2aero-gel/activated carbon composite materials for TNT solution is mainly surface adsorption, and also has some chemical adsorp-tion when the aerogel hydrophobicity is modified.

  8. Effects of Igneous Intrusion on Microporosity and Gas Adsorption Capacity of Coals in the Haizi Mine, China

    OpenAIRE

    Jingyu Jiang; Yuanping Cheng

    2014-01-01

    This paper describes the effects of igneous intrusions on pore structure and adsorption capacity of the Permian coals in the Huaibei Coalfield, China. Twelve coal samples were obtained at different distances from a ~120 m extremely thick sill. Comparisons were made between unaltered and heat-affected coals using geochemical data, pore-fracture characteristics, and adsorption properties. Thermal alteration occurs down to ~1.3 × sill thickness. Approaching the sill, the vitrinite reflectance (R...

  9. Effectiveness of Alkali-Acid Treatment in Enhancement the Adsorption Capacity for Rice Straw: The Removal of Methylene Blue Dye

    OpenAIRE

    Nady A. Fathy; El-Shafey, Ola I.; Khalil, Laila B.

    2013-01-01

    The effectiveness of alkali-acid modification in enhancement the adsorption capacity of rice straw (RS) for removing a basic dye was studied. The obtained adsorbents were characterized by slurry pH, pHPZC, iodine number, methylene blue number, FTIR, and SEM analyses. Adsorption of methylene blue (MB) was described by the Langmuir, Freundlich, Tempkin, and Redlich-Peterson isotherm models. Effects of contact time, initial concentration of MB dye, pH of solution, adsorbent dose, salt concentrat...

  10. Reservoir capacity estimates in shale plays based on experimental adsorption data

    Science.gov (United States)

    Ngo, Tan

    from different measurement techniques using representative fluids (such as CH4 and CO2) at elevated pressures, and the adsorbed density can range anywhere between the liquid and the solid state of the adsorbate. Whether these discrepancies are associated with the inherent heterogeneity of mudrocks and/or with poor data quality requires more experiments under well-controlled conditions. Nevertheless, it has been found in this study that methane GIP estimates can vary between 10-45% and 10-30%, respectively, depending on whether the free or the total amount of gas is considered. Accordingly, CO2 storage estimates range between 30-90% and 15-50%, due to the larger adsorption capacity and gas density at similar pressure and temperature conditions. A manometric system has been designed and built that allows measuring the adsorption of supercritical fluids in microporous materials. Preliminary adsorption tests have been performed using a microporous 13X zeolite and CO 2 as an adsorbing gas at a temperature of 25oC and 35oC and at pressures up to 500 psi. Under these conditions, adsorption is quantified with a precision of +/- 3%. However, relative differences up to 15-20% have been observed with respect to data published in the literature on the same adsorbent and at similar experimental conditions. While it cannot be fully explained with uncertainty analysis, this discrepancy can be reduced by improving experiment practice, thus including the application of a higher adsorbent's regeneration temperature, of longer equilibrium times and of a careful flushing of the system between the various experimental steps. Based on the results on 13X zeolite, virtual tests have been conducted to predict the performance of the manometric system to measure adsorption on less adsorbing materials, such as mudrocks. The results show that uncertainties in the estimated adsorbed amount are much more significant in shale material and they increase with increasing pressure. In fact, relative

  11. Enhancing adsorption capacity of toxic malachite green dye through chemically modified breadnut peel: equilibrium, thermodynamics, kinetics and regeneration studies.

    Science.gov (United States)

    Chieng, Hei Ing; Lim, Linda B L; Priyantha, Namal

    2015-01-01

    Breadnut skin, in both its unmodified (KS) and base-modified (BM-KS) forms, was investigated for its potential use as a low-cost adsorbent for the removal of toxic dye, malachite green (MG). Characterization of the adsorbents was carried out using scanning electron microscope, X-ray fluorescence and Fourier transform infra-red spectroscopy. Batch adsorption experiments, carried out under optimized conditions, for the adsorption of MG were fitted using five isotherm models (Langmuir, Freundlich, Dubinin-Radushkevich, Temkin and Sips) and six error functions to determine the best-fit model. The adsorption capacity was greatly enhanced when breadnut skin was chemically modified with NaOH, leading to an adsorption capacity of 353.0 mg g(-1), that was far superior to most reported adsorbents for the removal of MG. Thermodynamics studies indicated that the adsorption of MG was spontaneous on KS and BM-KS, and the reactions were endothermic and exothermic, respectively. Kinetics studies showed that both followed the pseudo-second order. Regeneration experiments on BM-KS indicated that its adsorption capacity was still maintained at>90% even after five cycles. It can be concluded that NaOH-modified breadfruit skin has great potential to be utilized in real-life application as a low-cost adsorbent for the removal of MG in wastewater treatment.

  12. Preparation of mesoporous poly (acrylic acid)/SiO2 composite nanofiber membranes having adsorption capacity for indigo carmine dye

    Science.gov (United States)

    Xu, Ran; Jia, Min; Li, Fengting; Wang, Hongtao; Zhang, Bingru; Qiao, Junlian

    2012-03-01

    Mesoporous poly (acrylic acid)/SiO2 (PAA/SiO2) composite nanofiber membranes functionalized with mercapto groups were fabricated by a sol-gel electrospinning method, and their adsorption capacity for indigo carmine was investigated. The membranes were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, x-ray powder diffraction (XRD), and nitrogen adsorption-desorption measurement. SEM and TEM observation results showed that the PAA/SiO2 fibers had diameters between 400-800 nm and mesopores with an average pore size of 3.88 nm. The specific surface area of the mesoporous nanofiber membranes was 514.89 m2/g. The characteristic peaks for mercapto group vibration in FTIR and Raman spectra demonstrated that the mercapto groups have been incorporated into the silica skeleton. The adsorption isotherm data of indigo carmine on the membranes fit well with Redlich-Peterson model, and the maximum adsorption capacity calculated was 523.11 mg/g. It was found that the removal rate of indigo carmine by the membranes reached a maximum of 98% in 90 min and the adsorption kinetics followed a pseudo-second-order model. The high adsorption capacity of PAA/SiO2 nanofiber membrane makes it a promising adsorbent for indigo carmine removal from the wastewater.

  13. Preparation of a porous clay heterostructure and study of its adsorption capacity of phenol and chlorinated phenols from aqueous solutions.

    Science.gov (United States)

    Arellano-Cárdenas, Sofía; Gallardo-Velázquez, Tzayhrí; Osorio-Revilla, Guillermo; López-Cortez, Ma del Socorro

    2008-01-01

    A porous clay heterostructure (PCH) from a Mexican clay was prepared and characterized, and its aqueous phenol and dichlorophenols (DCPs) adsorption capacities were studied using a batch equilibrium technique. The PCH displayed a surface area of 305.5 m2/g, 37.2 A average porous diameter, and a basal space of 23.2 A. The adsorption capacity shown by the PCH for both phenol and DCPs from water (14.5 mg/g for phenol; 48.7 mg/g for 3,4-DCP; and 45.5 mg/g for 2,5-DCP) suggests that the PCH has both hydrophobic and hydrophilic characteristics, as a result of the presence of silanol and siloxane groups formed during the pillaring and calcination of the PCH. The values of maximal adsorption capacity for dichlorophenols were higher than those reported for aluminum pillared clays and some inorgano-organo clays and comparable with some ionic exchange resins.

  14. The adsorption behavior of mercury on the hematite (1-102) surface from coal-fired power plant emissions

    Science.gov (United States)

    Jung, J. E.; Jew, A. D.; Rupp, E.; Aboud, S.; Brown, G. E.; Wilcox, J.

    2014-12-01

    One of the biggest environmental concerns caused by coal-fired power plants is the emission of mercury (Hg). Worldwide, 475 tons of Hg are released from coal-burning processes annually, comprising 24% of total anthropogenic Hg emissions. Because of the high toxicity of Hg species, US Environmental Protection Agency (EPA) proposed a standard on Hg and air toxic pollutants (Mercury and Air Toxics Standards, MATS) for new and existing coal-fired power plants in order to eliminate Hg in flue gas prior to release through the stack. To control the emission of Hg from coal-derived flue gas, it is important to understand the behavior, speciation of Hg as well as the interaction between Hg and solid materials, such as fly ash or metal oxides, in the flue gas stream. In this study, theoretical investigations using density functional theory (DFT) were carried out in conjunction with experiments to investigate the adsorption behavior of oxidized Hg on hematite (α-Fe2O3), an important mineral component of fly ash which readily sorbes Hg from flue gas. For DFT calculation, the two α-Fe2O3 (1-102) surfaces modeled consisted of two different surface terminations: (1) M2-clean, which corresponds to the oxygen-terminated surface with the first layer of cations removed and with no hydroxyl groups and (2) M2-OH2-OH, which has bihydroxylated top oxygen atoms and a second layer of hydroxylated oxygen atoms. These surface terminations were selected because both surfaces are highly stable in the temperature range of flue gases. The most probable adsorption sites of Hg, Cl and HgCl on the two α-Fe2O3 surface terminations were suggested based on calculated adsorption energies. Additionally, Bader charge and projected density of states (PDOS) analyses were conducted to characterize the oxidation state of adsorbates and their bonding interactions with the surfaces. Results indicate that oxidized Hg physically adsorbs on the M2-clean surface with a binding energy of -0.103 eV and that

  15. Synthesis of polycationic bentonite-ionene complexes and their benzene adsorption capacity

    Directory of Open Access Journals (Sweden)

    Valquíria Campos

    2015-04-01

    Full Text Available The purpose of this work was to structurally modify clays in order to incorporate water-insoluble molecules, such as petroleum hydrocarbons. The potential for ion exchange of quaternary ammonium salts was studied, which revealed their ability to interact with anions on the cationic surface, for environmental applications of the material. Ionenes, also known as polycations, have many potential uses in environmental applications. In this work, cationic aliphatic ammonium polyionenes, specifically 3,6-ionene and 3,6-dodecylionene, were prepared for incorporation into clay to form bentonite-ionene complexes. The intercalation of bentonite with ionene polymers resulted in an increase in the basal spacing of 3,6-dodecylionene from 1.5-3.5 nm. The higher d001 spacing of 3,6-dodecylionene samples than that of 3,6-ionene samples may be attributed to their longer tail length. The behavior of the TG/DTG curves and the activation energy values suggest that 3,6-dodecylionene (E = 174.85 kJ mol–1 is thermally more stable than 3,6 ionene (E = 115.52 kJ mol–1 complexes. The adsorption of benzene by 3,6-ionene and 3,6-dodecylionene was also investigated. The increase in benzene concentrations resulted in increased benzene adsorption by the sorbents tested in this work. The sorption capacity of benzene on ionene-modified bentonite was in the order of 3,6-dodecylionene > 3,6-ionene.

  16. Porphyrin-Alkaline Earth MOFs with the Highest Adsorption Capacity for Methylene Blue.

    Science.gov (United States)

    Hou, Yuxia; Sun, Junshan; Zhang, Daopeng; Qi, Dongdong; Jiang, Jianzhuang

    2016-04-25

    A series of four porphyrin-alkaline earth metal- organic frameworks [Mg(HDCPP)2 (DMF)2 ]n ⋅(H2 O)7 n (1), [Ca(HDCPP)2 (H2 O)2 ]n (DMF)1.5 n (2), [Sr(DCPP)(H2 O)(DMA)]n (3), and [Ba(DCPP)(H2 O)(DMA)]n (4) was isolated for the first time from solvothermal reaction between metal-free 5,15-di(4- carboxyphenyl)porphyrin (H2 DCPP) and alkaline earth ions. Single-crystal X-ray diffraction analysis reveals the 2D and 3D supramolecular network with periodic nanosized porosity for 1/2 and 3/4, respectively. The whole series of MOFs, in particular, compounds 1 and 2 with intrinsic low molecular formula weight, exhibit superior adsorption performance for methylene blue (MB) with excellent capture capacity as represented by the thus far highest adsorption amount of 952 mg g(-1) for 2 and good selectivity, opening a new way for the potential application of the main group metal-based MOFs. PMID:27002679

  17. Fiber-based adsorbents having high adsorption capacities for recovering dissolved metals and methods thereof

    Energy Technology Data Exchange (ETDEWEB)

    Janke, Christopher J.; Dai, Sheng; Oyola, Yatsandra

    2016-09-06

    A fiber-based adsorbent and a related method of manufacture are provided. The fiber-based adsorbent includes polymer fibers with grafted side chains and an increased surface area per unit weight over known fibers to increase the adsorption of dissolved metals, for example uranium, from aqueous solutions. The polymer fibers include a circular morphology in some embodiments, having a mean diameter of less than 15 microns, optionally less than about 1 micron. In other embodiments, the polymer fibers include a non-circular morphology, optionally defining multiple gear-shaped, winged-shaped or lobe-shaped projections along the length of the polymer fibers. A method for forming the fiber-based adsorbents includes irradiating high surface area polymer fibers, grafting with polymerizable reactive monomers, reacting the grafted fibers with hydroxylamine, and conditioning with an alkaline solution. High surface area fiber-based adsorbents formed according to the present method demonstrated a significantly improved uranium adsorption capacity per unit weight over existing adsorbents.

  18. Biomimetic mineralization of nano-sized, needle-like hydroxyapatite with ultrahigh capacity for lysozyme adsorption.

    Science.gov (United States)

    Ma, Yi; Zhang, Juan; Guo, Shanshan; Shi, Jie; Du, Wenying; Wang, Zheng; Ye, Ling; Gu, Wei

    2016-11-01

    Because of its superior biocompatibility, hydroxyapatite (HA) has been widely exploited as a promising vehicle to deliver a broad range of therapeutics in a variety of biological systems. Herein, we report a biomimetic process to prepare nano-sized, colloidal stable HA with needle-like morphology by using carboxymethyl cellulose (CMC) as the template. It was revealed that the needle-like HA was transformed from the spherical amorphous calcium phosphate (ACP) nanoparticles after a 14-day period of aging under ambient conditions. The needle-like HA/CMC exhibited an ultra-high lysozyme adsorption capacity up to 930-940mg/g. Moreover, a sustained and pH-sensitive release of adsorbed lysozyme from HA/CMC was evidenced. Therefore, our biomimetic needle-like HA/CMC nanoparticles hold great potential in serving as an efficient carrier for the delivery and controlled release of lysozyme. PMID:27524053

  19. ADSORPTION CAPACITY OF ACTIVATED CARBON FIBER FABRIC IN CYANIDE LEACHING LIQUOR OF GOLD ORES

    Institute of Scientific and Technical Information of China (English)

    LIUXiaozhen

    2002-01-01

    Adsorption capacity of ACFF in cyanide leaching liquor of gold ores was studied with cyanide leaching liquor of gold ores,containing various kinds of ions.The adsorbed leaching liquor was analyzed by atomic emission spectroscopy and colorimetric method.The contents of various kinds. of ions in ACFF were determined with X-ray photoctron spectroscopy.ACFF not only adsorbed gold but also adsorbed arsenic,nickel,zinc,calcium,sulphur,bismuth,copper,iron,silver and cyanide,anion.Atomic percentage of C and those of O,N,Zn,Fe increase and decrease respectively with the increase of the layer depth,while those of Ca,Au,Ag keep constant.

  20. In-Situ Ligand Formation-Driven Preparation of a Heterometallic Metal-Organic Framework for Highly Selective Separation of Light Hydrocarbons and Efficient Mercury Adsorption.

    Science.gov (United States)

    Han, Yi; Zheng, Hao; Liu, Kang; Wang, Hongli; Huang, Hongliang; Xie, Lin-Hua; Wang, Lei; Li, Jian-Rong

    2016-09-01

    By means of the in situ ligand formation strategy and hard-soft acid-base (HSAB) theory, two types of independent In(COO)4 and Cu6S6 clusters were rationally embedded into the heterometallic metal-organic framework (HMOF) {[(CH3)2NH2]InCu4L4·xS}n (BUT-52). BUT-52 exhibits a three-dimensional (3D) anionic framework structure and has sulfur decorating the dumbbell-shaped cages with the external edges of 24 and 14 Å by the internal edges. Remarkably, because of the stronger charge-induced interactions between the charged MOF skeleton and the easily polarized C2 hydrocarbons (C2s), BUT-52 was used for C2s over CH4 and shows both high adsorption heats of C2s and selective separation abilities for C2s/CH4. Furthermore, BUT-52 also displays efficient mercury adsorption resulting from the stronger-binding ability beween the sulfur and the mercury and can remove 92% mercury from methanol solution even with the initial concentration as low as 100 mg/L. The results in this work indicate the feasibility of BUT-52 for the separation of light hydrocarbons and efficient adsorption/removal of mercury. PMID:27548083

  1. Copper Accumulation, Availability and Adsorption Capacity in Sandy Soils of Vineyards with Different Cultivation Duration

    Science.gov (United States)

    Mallmann, F. J. K.; Miotto, A.; Bender, M. A.; Gubiani, E.; Rheinheimer, D. D. S.; Kaminski, J.; Ceretta, C. A.; Šimůnek, J.

    2015-12-01

    Bordeaux mixture is a copper-based (Cu) fungicide and bactericide applied in vineyards to control plant diseases. Since it is applied several times per year, it accumulates in large quantities on plants and in soil. This study evaluates the Cu accumulation in, and desorption kinetics and adsorption capability of a sandy Ultisol in a natural field and in 3 vineyards for 5 (V1), 11 (V2), and 31 (V3) years in South of Brazil. Soil samples were collected in 8 depths (0-60 cm) of all four soil profiles, which all displayed similar soil properties. The following soil properties were measured: pH, organic matter (OM), soil bulk density, Cu total concentration, and Cu desorption and adsorption curves. A two first-order reactions model and the Langmuir isotherm were fitted to the desorption and adsorption curves, respectively. An increase in the total mass of Cu in the vineyards followed a linear regression curve, with an average annual increase of 7.15 kg ha-1. Cu accumulated down to a depth of 5, 20, and 30 cm in V1, V2 and V3, respectively, with the highest Cu content reaching 138.4 mg kg-1 in the 0-5 cm soil layer of V3. Cu desorption parameters showed a high correlation with its total concentration. Approximately 57 and 19% of total Cu were immediately and slowly available, respectively, indicating a high potential for plant absorption and/or downward movement. Cu concentrations extracted by EDTA from soil layers not affected by anthropogenic Cu inputs were very low. The maximum Cu adsorption capacity of the 0-5 and 5-10 cm soil layers increased with the vineyard age, reaching concentrations higher than 900 mg kg-1. This increase was highly related to OM and pH, which both increased with cultivation duration. Despite of low clay content of these soils, there is low risk of groundwater Cu contamination for actual conditions. However, high Cu concentrations in the surface layer of the long-term vineyards could cause toxicity problems for this and for companion crops.

  2. Changing the adsorption capacity of coal-based honeycomb monoliths for pollutant removal from liquid streams by controlling their porosity

    International Nuclear Information System (INIS)

    Coal-based honeycomb monoliths extruded using methods developed for ceramic materials have been used to retain methylene blue and p-nitrophenol from aqueous solutions. The influence of the filters' thermal treatment on their textural properties and performance as adsorbents was examined. Characterization by N2 physisorption, mercury porosimetry and scanning electron microscopy along with adsorption tests under dynamic conditions suggest that, depending on the pollutant and its initial concentration, it can be more convenient to previously submit the monoliths to a simple carbonization or to an additional activation, with or without preoxidation, as a consequence of their different resulting pore structures. Infrared spectroscopy indicates that their different adsorption behaviour seems not to be related to differences in their surface chemical groups. In addition, axial crushing tests show that the monoliths have an acceptable mechanical resistance for the application investigated.

  3. Response to Comment on “Modeling Maximum Adsorption Capacities of Soot and Soot-like Materials for PAHs and PCBs”

    NARCIS (Netherlands)

    Noort, van P.C.M.; Jonker, M.T.O.; Koelmans, A.A.

    2005-01-01

    A comment by John C. Fetzer on modeling maximum adsorption capacities of soot and soot-like materials for PAH and PCB and the adsorption behavior of PAH on soots and on other adsorptive materials is presented. The authors (van Noort et al.) base their model on van der Waal's forces only. This may be

  4. Synthesis, characterisation and adsorption properties of a porous copper(II) 3D coordination polymer exhibiting strong binding enthalpy and adsorption capacity for carbon dioxide.

    Science.gov (United States)

    Eckold, Pierre; Gee, William J; Hill, Matthew R; Batten, Stuart R

    2012-11-21

    The synthesis and characterisation of microporous coordination polymers containing copper(II) or cobalt(II) and 2-(pyridin-4-yl)malonaldehyde (Hpma) is described and the gas adsorption properties evaluated. Single-crystal X-ray structure determinations identified the structures as [M(pma)(2)]·2X (M = Cu, 1; Co, 2; X = MeOH, MeCN), which contain 3D networks with rutile topology and continuous 1D rectangular channels with diameters ranging from 3 to 4 Å. The materials exhibit low BET surface areas of 143 m(2) g(-1), but possess large capacities for carbon dioxide capture of 14.1 wt%. The small pore channels are shown to account for this, delivering a particularly strong binding enthalpy to adsorbed CO(2) of 38 kJ mol(-1), and a very large adsorption capacity relative to the low surface area.

  5. Surface-Energetic Heterogeneity of Nanoporous Solids for CO2 and CO Adsorption: The Key to an Adsorption Capacity and Selectivity at Low Pressures.

    Science.gov (United States)

    Kim, Moon Hyeon; Cho, Il Hum; Choi, Sang Ok; Lee, In Soo

    2016-05-01

    This study has been focused on surface energetic heterogeneity of zeolite (H-mordenite, "HM"), activated carbon ("RB2") and metal-organic framework family ("Z1200") materials and their isotherm features in adsorption of CO2 and CO at 25 degrees C and low pressures ≤ 850 Torr. The nanoporous solids showed not only distinctive shape of adsorption isotherms for CO2 with relatively high polarizability and quadrupole moment but also different capacities in the CO2 adsorption. These differences between the adsorbents could be well correlated with their surface nonuniformity. The most heterogeneous surfaces were found with the HM that gave the highest CO2 uptake at all pressures allowed, while the Z1200 consisted of completely homogeneous surfaces and even CO2 adsorption linearly increased with pressure. An intermediate character was indicated on the surface of RB2 and thus this sorbent possessed isotherm features between the HM and Z1200 in CO2 adsorption. Such different surface energetics was fairly consistent with changes in CO2/CO selectivity on the nanoporous adsorbents up to equilibrated pressures near 850 Torr. PMID:27483776

  6. High adsorption capacity of heavy metals on two-dimensional MXenes: an ab initio study with molecular dynamics simulation.

    Science.gov (United States)

    Guo, Xun; Zhang, Xitong; Zhao, Shijun; Huang, Qing; Xue, Jianming

    2016-01-01

    Density functional theory (DFT) calculation is employed to study the adsorption properties of Pb and Cu on recently synthesized two-dimensional materials MXenes, including Ti3C2, V2C1 and Ti2C1. The influence of surface decoration with functional groups such as H, OH and F have also been investigated. Most of these studied MXenes exhibit excellent capability to adsorb Pb and Cu, especially the adsorption capacity of Pb on Ti2C1 is as high as 2560 mg g(-1). Both the binding energies and the adsorption capacities are sensitive to the functional groups attached to the MXenes' surface. Ab initio molecular dynamics (ab-init MD) simulation confirms that Ti2C1 remains stable at room temperature after adsorbing Pb atoms. Our calculations imply that these newly emerging two-dimensional MXenes are promising candidates for wastewater treatment and ion separation. PMID:26602974

  7. Integrated Removal of NOx with Carbon Monoxide as Reductant, and Capture of Mercury in a Low Temperature Selective Catalytic and Adsorptive Reactor

    Energy Technology Data Exchange (ETDEWEB)

    Neville Pinto; Panagiotis Smirniotis; Stephen Thiel

    2010-08-31

    Coal will likely continue to be a dominant component of power generation in the foreseeable future. This project addresses the issue of environmental compliance for two important pollutants: NO{sub x} and mercury. Integration of emission control units is in principle possible through a Low Temperature Selective Catalytic and Adsorptive Reactor (LTSCAR) in which NO{sub x} removal is achieved in a traditional SCR mode but at low temperature, and, uniquely, using carbon monoxide as a reductant. The capture of mercury is integrated into the same process unit. Such an arrangement would reduce mercury removal costs significantly, and provide improved control for the ultimate disposal of mercury. The work completed in this project demonstrates that the use of CO as a reductant in LTSCR is technically feasible using supported manganese oxide catalysts, that the simultaneous warm-gas capture of elemental and oxidized mercury is technically feasible using both nanostructured chelating adsorbents and ceria-titania-based materials, and that integrated removal of mercury and NO{sub x} is technically feasible using ceria-titania-based materials.

  8. Efficient Removal of Co2+ from Aqueous Solution by 3-Aminopropyltriethoxysilane Functionalized Montmorillonite with Enhanced Adsorption Capacity

    Science.gov (United States)

    Huang, Zhujian; Gong, Beini; Dai, Yaping; Chiang, Pen-Chi; Lai, Xiaolin; Yu, Guangwei

    2016-01-01

    To achieve a satisfactory removal efficiency of heavy metal ions from wastewater, silane-functionalized montmorillonite with abundant ligand-binding sites (-NH2) was synthesized as an efficient adsorbent. Ca-montmorillonite (Ca-Mt) was functionalized with 3-aminopropyl triethoxysilane (APTES) to obtain the APTES-Mt products (APTES1.0CEC-Mt, APTES2.0CEC-Mt, APTES3.0CEC-Mt, APTES4.0CEC-Mt) with enhanced adsorption capacity for Co2+. The physico-chemical properties of the synthesized adsorbents were characterized by spectroscopic and microscopic methods, and the results demonstrated that APTES was successfully intercalated into the gallery of Ca-Mt or grafted onto the surface of Ca-Mt through Si-O bonds. The effect of solution pH, ionic strength, temperature, initial concentrations and contact time on adsorption of Co2+ by APTES-Mt was evaluated. The results indicated that adsorption of Co2+ onto Ca-Mt, APTES1.0CEC-Mt and APTES2.0CEC-Mt can be considered to be a pseudo-second-order process. In contrast, adsorption of Co2+ onto APTES3.0CEC-Mt and APTES4.0CEC-Mt fitted well with the pseudo-first-order kinetics. The adsorption isotherms were described by the Langmuir model, and the maximum adsorption capacities of APTES1.0CEC-Mt, APTES2.0CEC-Mt, APTES3.0CEC-Mt and APTES4.0CEC-Mt were 25.1, 33.8, 61.6, and 61.9 mg·g-1, respectively. In addition, reaction temperature had no impact on the adsorption capacity, while both the pH and ionic strength significantly affected the adsorption process. A synergistic effect of ion exchange and coordination interactions on adsorption was observed, thereby leading to a significant enhancement of Co2+ adsorption by the composites. Thus, APTES-Mt could be a cost-effective and environmental-friendly adsorbent, with potential for treating Co2+-rich wastewater. PMID:27448094

  9. Efficient Removal of Co2+ from Aqueous Solution by 3-Aminopropyltriethoxysilane Functionalized Montmorillonite with Enhanced Adsorption Capacity.

    Science.gov (United States)

    Huang, Zhujian; Wu, Pingxiao; Gong, Beini; Dai, Yaping; Chiang, Pen-Chi; Lai, Xiaolin; Yu, Guangwei

    2016-01-01

    To achieve a satisfactory removal efficiency of heavy metal ions from wastewater, silane-functionalized montmorillonite with abundant ligand-binding sites (-NH2) was synthesized as an efficient adsorbent. Ca-montmorillonite (Ca-Mt) was functionalized with 3-aminopropyl triethoxysilane (APTES) to obtain the APTES-Mt products (APTES1.0CEC-Mt, APTES2.0CEC-Mt, APTES3.0CEC-Mt, APTES4.0CEC-Mt) with enhanced adsorption capacity for Co2+. The physico-chemical properties of the synthesized adsorbents were characterized by spectroscopic and microscopic methods, and the results demonstrated that APTES was successfully intercalated into the gallery of Ca-Mt or grafted onto the surface of Ca-Mt through Si-O bonds. The effect of solution pH, ionic strength, temperature, initial concentrations and contact time on adsorption of Co2+ by APTES-Mt was evaluated. The results indicated that adsorption of Co2+ onto Ca-Mt, APTES1.0CEC-Mt and APTES2.0CEC-Mt can be considered to be a pseudo-second-order process. In contrast, adsorption of Co2+ onto APTES3.0CEC-Mt and APTES4.0CEC-Mt fitted well with the pseudo-first-order kinetics. The adsorption isotherms were described by the Langmuir model, and the maximum adsorption capacities of APTES1.0CEC-Mt, APTES2.0CEC-Mt, APTES3.0CEC-Mt and APTES4.0CEC-Mt were 25.1, 33.8, 61.6, and 61.9 mg·g-1, respectively. In addition, reaction temperature had no impact on the adsorption capacity, while both the pH and ionic strength significantly affected the adsorption process. A synergistic effect of ion exchange and coordination interactions on adsorption was observed, thereby leading to a significant enhancement of Co2+ adsorption by the composites. Thus, APTES-Mt could be a cost-effective and environmental-friendly adsorbent, with potential for treating Co2+-rich wastewater.

  10. Mercury Removal from Aqueous Solution and Flue Gas by Adsorption on Activated Carbon Fibres

    OpenAIRE

    Nabais, Joao; Carrott, Peter; Ribeiro Carrott, Manuela

    2006-01-01

    The use of two activated carbon fibres, one laboratorial sample prepared from a commercial acrylic textile fibre and one commercial sample of Kynol1, as prepared/received and modified by reaction with powdered sulfur and H2S gas in order to increase the sulfur content were studied for the removal of mercury from aqueous solution and from flue gases from a fluidized bed combustor. The sulfur introduced ranged from 1 to 6 wt.% depending on the method used. The most important parameter ...

  11. Preparation of Urea Nitrogen Adsorbent of Complex Type and Adsorption Capacity of Urea Nitrogen onto the Adsorbent

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The urea nitroge n adsorbent of complex type, which consists of chitosan coated dialdehyde cellulose (CDAC) and immobilized urease in gelatin membrane (IE), was prepared. The cellulose, the dialdehyde cellulose (DAC) and the CDAC were characterized by scanning electronic microscope. The results indicate that the cellulose C2-C3 bond was broken under the oxidation of periodate and it was oxidated to DAC. The DAC was coated with chitosan and the CDAC was obtained. The adsorption of urea nitrogen onto the adsorbent in Na2HPO4-NaH2PO4 buffer solution was studied in batch system. The effects of the experiment parameters, including degree of oxidation of CDAC, initial urea nitrogen concentration, pH and temperature, on the adsorption capacity of urea nitrogen onto the adsorbent at CDAC/IE weight ratio 10:1 were investigated. The results indicate that these parameters affected significantly the adsorption capacity. The adsorption capacity of urea nitrogen onto the adsorbent was 36.7 mg/g at the degree of oxidation of CDAC 88%, initial urea nitrogen concentration 600 mg/L, pH 7.4 and temperature 37 ℃.

  12. Mercury species, selenium, metallothioneins and glutathione in two dolphins from the southeastern Brazilian coast: Mercury detoxification and physiological differences in diving capacity.

    Science.gov (United States)

    Kehrig, Helena A; Hauser-Davis, Rachel A; Seixas, Tercia G; Pinheiro, Ana Beatriz; Di Beneditto, Ana Paula M

    2016-06-01

    In the present study, the concentration of trace elements, total mercury (Hg) and selenium (Se) and mercury forms (MeHg, Hginorg and HgSe) in the vulnerable coastal dolphins Pontoporia blainvillei and Sotalia guianensis were appraised and compared, using metallothioneins (MT) and glutathione (GSH) as biomarkers for trace element exposure. The trace element concentrations varied between muscle and liver tissues, with liver of all dolphin specimens showing higher Hg and Se concentrations than those found in muscle. Hg, MeHg and Hginorg molar concentrations showed a clear increase with Se molar concentrations in the liver of both dolphins, and Se concentrations were higher than those of Hg on a molar basis. Se plays a relevant role in the detoxification of MeHg in the hepatic tissue of both dolphins, forming Hg-Se amorphous crystals in liver. In contrast, MT were involved in the detoxification process of Hginorg in liver. GSH levels in P. blainvillei and S. guianensis muscle tissue suggest that these dolphins have different diving capacities. Muscle Hg concentrations were associated to this tripeptide, which protects dolphin cells against Hg stress. PMID:27038210

  13. Determination of Xanthine in the Presence of Hypoxanthine by Adsorptive Stripping Voltammetry at the Mercury Film Electrode

    Science.gov (United States)

    Farias, Percio Augusto Mardini; Castro, Arnaldo Aguiar

    2014-01-01

    A stripping method for the determination of xanthine in the presence of hypoxanthine at the submicromolar concentration levels is described. The method is based on controlled adsorptive accumulation at the thin-film mercury electrode followed by a fast linear scan voltammetric measurement of the surface species. Optimum experimental conditions were found to be the use of 1.0 × 10−3 mol L−1 NaOH solution as supporting electrolyte, an accumulation potential of 0.00 V for xanthine and −0.50 V for hypoxanthine–copper, and a linear scan rate of 200 mV second−1. The response of xanthine is linear over the concentration ranges of 20–140 ppb. For an accumulation time of 30 minutes, the detection limit was found to be 36 ppt (2.3 × 10−10 mol L−1). Adequate conditions for measuring the xanthine in the presence of hypoxanthine, copper and other metals, uric acid, and other nitrogenated bases were also investigated. The utility of the method is demonstrated by the presence of xanthine associated with hypoxanthine, uric acid, nitrogenated bases, ATP, and ssDNA. PMID:24940040

  14. Effects of textural and surface characteristics of microporous activated carbons on the methane adsorption capacity at high pressures

    Energy Technology Data Exchange (ETDEWEB)

    Bastos-Neto, M. [Grupo de Pesquisas em Separacoes por Adsorcao (GPSA), Departamento de Engenharia Quimica, Universidade Federal do Ceara, Campus Universitario do Pici, Bl 709 60455-760 Fortaleza, CE (Brazil); Canabrava, D.V. [Grupo de Pesquisas em Separacoes por Adsorcao (GPSA), Departamento de Engenharia Quimica, Universidade Federal do Ceara, Campus Universitario do Pici, Bl 709 60455-760 Fortaleza, CE (Brazil); Torres, A.E.B. [Grupo de Pesquisas em Separacoes por Adsorcao (GPSA), Departamento de Engenharia Quimica, Universidade Federal do Ceara, Campus Universitario do Pici, Bl 709 60455-760 Fortaleza, CE (Brazil); Rodriguez-Castellon, E. [Departamento de Quimica Inorganica, Cristalografia y Mineralogia (Unidad Asociada al ICP-CSIC), Facultad de Ciencias, Universidad de Malaga, 29071 Malaga (Spain); Jimenez-Lopez, A. [Departamento de Quimica Inorganica, Cristalografia y Mineralogia (Unidad Asociada al ICP-CSIC), Facultad de Ciencias, Universidad de Malaga, 29071 Malaga (Spain); Azevedo, D.C.S. [Grupo de Pesquisas em Separacoes por Adsorcao (GPSA), Departamento de Engenharia Quimica, Universidade Federal do Ceara, Campus Universitario do Pici, Bl 709 60455-760 Fortaleza, CE (Brazil)]. E-mail: diana@gpsa.ufc.br; Cavalcante, C.L. [Grupo de Pesquisas em Separacoes por Adsorcao (GPSA), Departamento de Engenharia Quimica, Universidade Federal do Ceara, Campus Universitario do Pici, Bl 709 60455-760 Fortaleza, CE (Brazil)

    2007-04-30

    The objective of this study is to relate textural and surface characteristics of selected microporous activated carbons to their methane storage capacity. In this work, a magnetic suspension balance (Rubotherm, Germany) was used to measure methane adsorption isotherms of several activated carbon samples. Textural characteristics were assessed by nitrogen adsorption on a regular surface area analyzer (Autosorb-MP, by Quantachrome, USA). N{sub 2} adsorption was analysed by conventional models (BET, DR, HK) and by Monte Carlo molecular simulations. Elemental and surface analyses were performed by X-ray photoelectronic spectroscopy (XPS) for the selected samples. A comparative analysis was then carried out with the purpose of defining some correlation among the variables under study. For the system under study, pore size distribution and micropore volume seem to be a determining factor as long as the solid surface is perfectly hydrophobic. It was concluded that the textural parameters per se do not unequivocally determine natural gas storage capacities. Surface chemistry and methane adsorption equilibria must be taken into account in the decision-making process of choosing an adsorbent for gas storage.

  15. Predicting CH4 adsorption capacity of microporous carbon using N2 isotherm and a new analytical model

    Science.gov (United States)

    Sun, Jielun; Chen, S.; Rostam-Abadi, M.; Rood, M.J.

    1998-01-01

    A new analytical pore size distribution (PSD) model was developed to predict CH4 adsorption (storage) capacity of microporous adsorbent carbon. The model is based on a 3-D adsorption isotherm equation, derived from statistical mechanical principles. Least squares error minimization is used to solve the PSD without any pre-assumed distribution function. In comparison with several well-accepted analytical methods from the literature, this 3-D model offers relatively realistic PSD description for select reference materials, including activated carbon fibers. N2 and CH4 adsorption data were correlated using the 3-D model for commercial carbons BPL and AX-21. Predicted CH4 adsorption isotherms, based on N2 adsorption at 77 K, were in reasonable agreement with the experimental CH4 isotherms. Modeling results indicate that not all the pores contribute the same percentage Vm/Vs for CH4 storage due to different adsorbed CH4 densities. Pores near 8-9 A?? shows higher Vm/Vs on the equivalent volume basis than does larger pores.

  16. Study of adsorption capacity of biomass for organic contaminants; Estudo da capacidade de adsorcao de biomassas para contaminantes organicos

    Energy Technology Data Exchange (ETDEWEB)

    Santos, E.G. [Universidade Federal de Campina Grande, PB (Brazil). Programa de Recursos Humanos da ANP, PRH-25]. E-mail: elbagomes@uol.com.br; Alsina, O.L.S.; Silva, F.L.H. [Universidade Federal de Campina Grande, PB (Brazil). Centro de Ciencias e Tecnologia. Dept. de Engenharia Quimica]. E-mail: odelsia@deq.ufpb.br; flhs@deq.ufpb.br

    2003-07-01

    Great amounts of water are found in the oil reservoirs associated to the oil generating many effluents. In the petroleum industry, the adsorption has been getting attention, because its efficiencies in the treatment of effluents. Adsorption had been proposed because their advantages when compared with other conventional purification process. Among the adsorbent materials, the biomass has a great importance due to the low cost presented. Experiments of organic pollutants adsorption were accomplished, using as biomass: corn-cob, wood powder and coconut mesocarp, in the natural forms and with acid treatment. In this paper, the behavior of the effluent with organic pollutant was simulated, by a dispersion of gas in water. By means of factorial experimental planning, it was possible to verify the influence of the input variables: gas initial concentration, amount of biomass and the system rotation, on the output variable; the adsorption capacity, as well as the effect of the acid treatment used. The results show that the most appropriate bioadsorbent for adsorption of organic pollutants was the coconut mesocarp. (author)

  17. Oxygen-induced Decrease in the Equilibrium Adsorptive Capacities of Activated Carbons

    OpenAIRE

    Ovín Ania, María Concepción; Parra Soto, José Bernardo; Pis Martínez, José Juan

    2004-01-01

    Special attention was paid in this work to the role of surface chemistry in the adsorption of phenol and salicylic acid onto activated carbons. To this end, two commercial activated carbons (granular and powdered) were oxidised using ammonium peroxodisulphate [(NH4) 2S2O8] and nitric acid in different concentrations. The structural and chemical properties of the oxidised adsorbents were characterised via nitrogen adsorption isotherms measured at –196 ° C and Boehm titrations. Phenol adsorptio...

  18. Experimental evidence for the influence of charge on the adsorption capacity of carbon dioxide on charged fullerenes

    CERN Document Server

    Ralser, Stefan; Probst, Michael; Postler, Johannes; Renzler, Michael; Bohme, Diethard K; Scheier, Paul

    2016-01-01

    We show, with both experiment and theory, that adsorption of $CO_2$ is sensitive to charge on a capturing model carbonaceous surface. In the experiment we dope superfluid helium droplets with $C_{60}$ and $CO_2$ and expose them to ionising free electrons. Both positively and negatively charged $C_{60}(CO_2)_n^{+/-}$ cluster ion distributions are observed with a high-resolution mass spectrometer and these show remarkable and reproducible anomalies in intensities that are strongly dependent on the charge. The highest adsorption capacity is seen with $C_{60}^+$. Complementary density functional theory calculations and molecular dynamics simulations provided insight into the nature of the interaction of charged $C_{60}$ with $CO_2$ as well as trends in the packing of $C_{60}^+$ and $C_{60}^-$. The quadrupole moment of $CO_2$ itself was seen to be decisive in determining the charge dependence of the observed adsorption features. Our findings are expected to apply to adsorption of $CO_2$ by charged surfaces in gene...

  19. The effects of pH on the adsorption of mercury on laterite from Guizhou Province, China

    Institute of Scientific and Technical Information of China (English)

    YU Xiaohong; ZHU Lijun; GUO Baiwei; LUO Yi

    2006-01-01

    In this paper, the role of pH value on the adsorption of Hg2+ on the laterite from Guizhou Province was studied. The lower pH is unfavorable to the adsorption of Hg2+ whereas the higher pH is favorable to the adsorption of Hg2+. When pH reached a certain value, the amount of Hg2+ adsorption reached the maximum. Then the amount of Hg2+ adsorption was reduced with increasing pH value.

  20. Effects of igneous intrusion on microporosity and gas adsorption capacity of coals in the Haizi Mine, China.

    Science.gov (United States)

    Jiang, Jingyu; Cheng, Yuanping

    2014-01-01

    This paper describes the effects of igneous intrusions on pore structure and adsorption capacity of the Permian coals in the Huaibei Coalfield, China. Twelve coal samples were obtained at different distances from a ~120 m extremely thick sill. Comparisons were made between unaltered and heat-affected coals using geochemical data, pore-fracture characteristics, and adsorption properties. Thermal alteration occurs down to ~1.3 × sill thickness. Approaching the sill, the vitrinite reflectance (R(o)) increased from 2.30% to 2.78%, forming devolatilization vacuoles and a fine mosaic texture. Volatile matter (VM) decreased from 17.6% to 10.0% and the moisture decreased from 3.0% to 1.6%. With decreasing distance to the sill, the micropore volumes initially increased from 0.0054 cm(3)/g to a maximum of 0.0146 cm(3)/g and then decreased to 0.0079 cm(3)/g. The results show that the thermal evolution of the sill obviously changed the coal geochemistry and increased the micropore volume and adsorption capacity of heat-affected coal (60-160 m from the sill) compared with the unaltered coals. The trap effect of the sill prevented the high-pressure gas from being released, forming gas pocket. Mining activities near the sill created a low pressure zone leading to the rapid accumulation of methane and gas outbursts in the Haizi Mine. PMID:24723841

  1. Effects of Igneous Intrusion on Microporosity and Gas Adsorption Capacity of Coals in the Haizi Mine, China

    Directory of Open Access Journals (Sweden)

    Jingyu Jiang

    2014-01-01

    Full Text Available This paper describes the effects of igneous intrusions on pore structure and adsorption capacity of the Permian coals in the Huaibei Coalfield, China. Twelve coal samples were obtained at different distances from a ~120 m extremely thick sill. Comparisons were made between unaltered and heat-affected coals using geochemical data, pore-fracture characteristics, and adsorption properties. Thermal alteration occurs down to ~1.3 × sill thickness. Approaching the sill, the vitrinite reflectance (Ro increased from 2.30% to 2.78%, forming devolatilization vacuoles and a fine mosaic texture. Volatile matter (VM decreased from 17.6% to 10.0% and the moisture decreased from 3.0% to 1.6%. With decreasing distance to the sill, the micropore volumes initially increased from 0.0054 cm3/g to a maximum of 0.0146 cm3/g and then decreased to 0.0079 cm3/g. The results show that the thermal evolution of the sill obviously changed the coal geochemistry and increased the micropore volume and adsorption capacity of heat-affected coal (60–160 m from the sill compared with the unaltered coals. The trap effect of the sill prevented the high-pressure gas from being released, forming gas pocket. Mining activities near the sill created a low pressure zone leading to the rapid accumulation of methane and gas outbursts in the Haizi Mine.

  2. Removal of Mercury from chlor-alkali Industry Wastewater using Acetobacter xylinum Cellulose

    Directory of Open Access Journals (Sweden)

    A. Rezaee

    2005-01-01

    Full Text Available In this study, the removal of mercury ions by cellulose of Acetobacter xylinum was investigated in the synthetic and chlor-alkali wastewater. Biofilms of Acetobacter xylinum were grown in laboratory column bioreactors. The biofilms were continuously treated with sterile synthetic model wastewater or nonsterile, neutralized chloralkali wastewater.The extent of adsorption was studied as function of pH, adsorbent dose and contact time. Efficiency of mercury ion removal from chlor-alkali industry wastewater by aluminum sulfate and ferric chloride was also determined. Under acidic condition the adsorption of mercury by cellulose was quite low and increasing processing time more than 10min has no remarkably effect on the adsorption rate. Adsorption capacity of cellulose under dynamic condition for chlor-alkali wastewater was 65mg/µg which was less than the value (80mg/µg that obtained from batch adsorption experiments for synthetic wastewater.

  3. An in vitro Study on the Adsorption, Absorption and Uptake Capacity of Zn by the Bioremediator Trichoderma atroviride

    Directory of Open Access Journals (Sweden)

    Mazyar Yazdani

    2010-01-01

    Full Text Available The concentrations of Zn in the sediment of a polluted river at the Serdang Industrial Area were determined. These polluted sediment samples revealed high level of Zn (219. 27 µg/g. Isolation of fungi from this polluted sediment was also carried out using Rose Bengal Agar (RBA. The isolated fungi were exposed to different concentrations of Zn (0-6000 mg/L on Potato Dextrose Agar (PDA to find the most tolerant isolate. Trichoderma atroviride was found to have the highest tolerance and it was studied for growth rate, Zn uptake capacity, its tolerance to Zn and also localization of Zn by using Potato Dextrose Broth (PDB as the liquid culture medium. In the present study the results found out that the uptake capacity of T. atroviride ranged from 18.1-26.7 mg/g in liquid media at Zn concentrations from 500 to 1000 mg/L. The isolate showed 47.6-64% adsorption and 30.4¬45.1% absorption for Zn. Based on the present study, 5.7-7.4% of Zn removal was observed due to biomass washing. The high adsorption, relatively low absorption and high uptake capacity of Zn suggest that T. atroviride is a potential bioremediator of Zn. However, further studies are needed to confirm its practical use as a bioremediating agent for Zn under field conditions.

  4. 2,4-D adsorption to biochars: effect of preparation conditions on equilibrium adsorption capacity and comparison with commercial activated carbon literature data.

    Science.gov (United States)

    Kearns, J P; Wellborn, L S; Summers, R S; Knappe, D R U

    2014-10-01

    Batch isotherm experiments were conducted with chars to study adsorption of the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D). Chars generated from corncobs, bamboo and wood chips in a laboratory pyrolyzer at 400-700 °C were compared with traditional kiln charcoals collected from villages in S/SE Asia and with activated carbons (ACs). 2,4-D uptake by laboratory chars obtained from bamboo and wood chips after 14 h of pyrolysis at 700 °C, from wood chips after 96 h of pyrolysis at 600 °C, and one of the field-collected chars (basudha) was comparable to ACs. H:C and O:C ratios declined with pyrolysis temperature and duration while surface area increased to >500 m(2)/g. Increasing pyrolysis intensity by increasing temperature and/or duration of heating was found to positively influence adsorption capacity yield (mg(2,4-D/g(feedstock))) over the range of conditions studied. Economic analysis showed that high temperature chars can be a cost-effective alternative to ACs for water treatment applications. PMID:24934321

  5. 2,4-D adsorption to biochars: effect of preparation conditions on equilibrium adsorption capacity and comparison with commercial activated carbon literature data.

    Science.gov (United States)

    Kearns, J P; Wellborn, L S; Summers, R S; Knappe, D R U

    2014-10-01

    Batch isotherm experiments were conducted with chars to study adsorption of the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D). Chars generated from corncobs, bamboo and wood chips in a laboratory pyrolyzer at 400-700 °C were compared with traditional kiln charcoals collected from villages in S/SE Asia and with activated carbons (ACs). 2,4-D uptake by laboratory chars obtained from bamboo and wood chips after 14 h of pyrolysis at 700 °C, from wood chips after 96 h of pyrolysis at 600 °C, and one of the field-collected chars (basudha) was comparable to ACs. H:C and O:C ratios declined with pyrolysis temperature and duration while surface area increased to >500 m(2)/g. Increasing pyrolysis intensity by increasing temperature and/or duration of heating was found to positively influence adsorption capacity yield (mg(2,4-D/g(feedstock))) over the range of conditions studied. Economic analysis showed that high temperature chars can be a cost-effective alternative to ACs for water treatment applications.

  6. Development of dry control technology for emissions of mercury in flue gas

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Hann S.; Wu, Jiann M.; Livengood, C.D.

    1995-06-01

    In flue gases from coal-combustion systems, mercury in either the elemental state or its chloride form (HgCl{sub 2}) can be predominant among all the possible mercury species present; this predominance largely depends on the chlorine-to-mercury ratio in the coal feeds. Conventional flue-gas cleanup technologies are moderately effective in controlling HgCl{sub 2} but are very poor at controlling elemental mercury. Experiments were conducted on the removal of elemental mercury vapor by means of a number of different types of sorbents, using a fixed-bed adsorption system. Of the four commercial activated carbons evaluated, the sulfur-treated carbon sample gives the best removal performance, with good mercury-sorption capacities. Promising removal results also have been obtained with low-cost minerals after chemical treatments. These inorganic sorbents could potentially be developed into a cost-effective alternative to activated carbons for mercury removal.

  7. 电石法聚氯乙烯含汞废水吸附除汞%Adsorption removal of mercury contained in wastewater from production of calcium carbide method PVC

    Institute of Scientific and Technical Information of China (English)

    王小昌; 李国栋

    2012-01-01

    Adsorption process for removing mercury was adopted to treat the mercury-containing wastewater released from the production of calcium carbide method PVC,and the mercury removing effects were investigated in an industrial plant.The results showed that this process could obtain good mercury removing effects,mercury content in mercury-containing wastewater could be reduced to less than 0.005 mg/L,the saturated adsorbent could be reused in adsorption mercury removing process after desorption,and the plant had characteristics of simple operation,steady running and little secondary pollution.%采用吸附除汞工艺对电石法聚氯乙烯生产过程中产生的含汞废水进行处理,通过工业化装置运行考察了除汞效果。结果表明:该工艺脱汞效果好,可以将含汞废水中的汞质量浓度降低到0.005mg/L以下,饱和吸附剂可经脱附处理后重新用于吸附除汞,且装置操作简单,运行稳定,不易产生二次污染。

  8. Evaluation of phosphorus adsorption capacity of sesame straw biochar on aqueous solution: influence of activation methods and pyrolysis temperatures.

    Science.gov (United States)

    Park, J H; Ok, Y S; Kim, S H; Cho, J S; Heo, J S; Delaune, R D; Seo, D C

    2015-12-01

    The phosphorus (P) adsorption characteristic of sesame straw biochar prepared with different activation agents and pyrolysis temperatures was evaluated. Between 0.109 and 0.300 mg L(-1) in the form of inorganic phosphate was released from raw sesame straw biochar in the first 1 h. The release of phosphate was significantly enhanced from 62.6 to 168.2 mg g(-1) as the pyrolysis temperature increased. Therefore, sesame straw biochar cannot be used as an adsorbent for P removal without change in the physicochemical characteristics. To increase the P adsorption of biochar in aqueous solution, various activation agents and pyrolysis temperatures were applied. The amount of P adsorbed from aqueous solution by biochar activated using different activation agents appeared in the order ZnCl2 (9.675 mg g(-1)) > MgO (8.669 mg g(-1)) ⋙ 0.1N-HCl > 0.1N-H2SO4 > K2SO4 ≥ KOH ≥ 0.1N-H3PO4, showing ZnCl2 to be the optimum activation agent. Higher P was adsorbed by the biochar activated using ZnCl2 under different pyrolysis temperatures in the order 600 °C > 500 °C > 400 °C > 300 °C. Finally, the amount of adsorbed P by activated biochar at different ratios of biochar to ZnCl2 appeared in the order 1:3 ≒ 1:1 > 3:1. As a result, the optimum ratio of biochar to ZnCl2 and pyrolysis temperature were found to be 1:1 and 600 °C for P adsorption, respectively. The maximum P adsorption capacity by activated biochar using ZnCl2 (15,460 mg kg(-1)) was higher than that of typical biochar, as determined by the Langmuir adsorption isotherm. Therefore, the ZnCl2 activation of sesame straw biochar was suitable for the preparation of activated biochar for P adsorption.

  9. Evaluation of phosphorus adsorption capacity of sesame straw biochar on aqueous solution: influence of activation methods and pyrolysis temperatures.

    Science.gov (United States)

    Park, J H; Ok, Y S; Kim, S H; Cho, J S; Heo, J S; Delaune, R D; Seo, D C

    2015-12-01

    The phosphorus (P) adsorption characteristic of sesame straw biochar prepared with different activation agents and pyrolysis temperatures was evaluated. Between 0.109 and 0.300 mg L(-1) in the form of inorganic phosphate was released from raw sesame straw biochar in the first 1 h. The release of phosphate was significantly enhanced from 62.6 to 168.2 mg g(-1) as the pyrolysis temperature increased. Therefore, sesame straw biochar cannot be used as an adsorbent for P removal without change in the physicochemical characteristics. To increase the P adsorption of biochar in aqueous solution, various activation agents and pyrolysis temperatures were applied. The amount of P adsorbed from aqueous solution by biochar activated using different activation agents appeared in the order ZnCl2 (9.675 mg g(-1)) > MgO (8.669 mg g(-1)) ⋙ 0.1N-HCl > 0.1N-H2SO4 > K2SO4 ≥ KOH ≥ 0.1N-H3PO4, showing ZnCl2 to be the optimum activation agent. Higher P was adsorbed by the biochar activated using ZnCl2 under different pyrolysis temperatures in the order 600 °C > 500 °C > 400 °C > 300 °C. Finally, the amount of adsorbed P by activated biochar at different ratios of biochar to ZnCl2 appeared in the order 1:3 ≒ 1:1 > 3:1. As a result, the optimum ratio of biochar to ZnCl2 and pyrolysis temperature were found to be 1:1 and 600 °C for P adsorption, respectively. The maximum P adsorption capacity by activated biochar using ZnCl2 (15,460 mg kg(-1)) was higher than that of typical biochar, as determined by the Langmuir adsorption isotherm. Therefore, the ZnCl2 activation of sesame straw biochar was suitable for the preparation of activated biochar for P adsorption. PMID:26040973

  10. An Analysis Of NH3 Adsorption Capacities of Natural And Pretreated Zeolites--EAC Presentation 2004

    OpenAIRE

    Reesa, Chee-Wah; Glass, Charles; Khunjar, Wendell; Sinclair, Hugh Berk

    2004-01-01

    This project plays a vital role which is to remove excess ammonia produced from the Solid Thermophilic Aerobic Reactor (STAR) system using a natural ion exchangers, zeolites. The analyses were carried out in laboratory scale batch reactors and column reactors. The preliminary batch studies showed that zeolites adsorbed ammonia at low concentrations with over 90% removal and the preliminary column study showed that zeolites had steep adsorption curves, which is effectual as resin media. The...

  11. Synthesis, characterisation and methyl orange adsorption capacity of ferric oxide-biochar nano-composites derived from pulp and paper sludge

    Science.gov (United States)

    Chaukura, Nhamo; Murimba, Edna C.; Gwenzi, Willis

    2016-02-01

    A Fe2O3-biochar nano-composite (Fe2O3-BC) was prepared from FeCl3-impregnated pulp and paper sludge (PPS) by pyrolysis at 750 °C. The characteristics and methyl orange (MO) adsorption capacity of Fe2O3-BC were compared to that of unactivated biochar (BC). X-ray diffraction (XRD) and scanning electron microscopy (SEM) confirmed the composite material was nano-sized. Fourier transform infrared (FTIR) spectroscopy revealed the presence of hydroxyl and aromatic groups on BC and on Fe2O3-BC, but Brunauer-Emmett-Teller (BET) surface area and Barrett-Joyner-Halenda (BJH) porosity were lower for Fe2O3-BC than BC. Despite the lower BET surface area and porosity of Fe2O3-BC, its MO adsorption capacity was 52.79 % higher than that of BC. The equilibrium adsorption data were best represented by the Freundlich model with a maximum adsorption capacity of 20.53 mg g-1 at pH 8 and 30 min contact time. MO adsorption obeyed pseudo-second-order kinetics for both BC and Fe2O3-BC with R 2 values of 0.996 and 0.999, respectively. Higher MO adsorption capacity for Fe2O3-BC was attributed to the hybrid nature of the nano-composites; adsorption occurred on both biochar matrix and Fe2O3 nanocrystals. Gibbs free energy calculations confirmed the adsorption is energetically favourable and spontaneous with a high preference for adsorption on both adsorbents. The nano-composite can be used for the efficient removal of MO (>97 %) from contaminated wastewater.

  12. Determination of coalbed methane potential and gas adsorption capacity in Western Kentucky coals

    Science.gov (United States)

    Mardon, S.M.; Takacs, K.G.; Hower, J.C.; Eble, C.F.; Mastalerz, Maria

    2006-01-01

    The Illinois Basin has not been developed for Coalbed Methane (CBM) production. It is imperative to determine both gas content and other parameters for the Kentucky portion of the Illinois Basin if exploration is to progress and production is to occur in this area. This research is part of a larger project being conducted by the Kentucky Geological Survey to evaluate the CBM production of Pennsylvanian-age western Kentucky coals in Ohio, Webster, and Union counties using methane adsorption isotherms, direct gas desorption measurements, and chemical analyses of coal and gas. This research will investigate relationships between CBM potential and petrographic, surface area, pore size, and gas adsorption isotherm analyses of the coals. Maceral and reflectance analyses are being conducted at the Center for Applied Energy Research. At the Indiana Geological Survey, the surface area and pore size of the coals will be analyzed using a Micrometrics ASAP 2020, and the CO2 isotherm analyses will be conducted using a volumetric adsorption apparatus in a water temperature bath. The aforementioned analyses will be used to determine site specific correlations for the Kentucky part of the Illinois Basin. The data collected will be compared with previous work in the Illinois Basin and will be correlated with data and structural features in the basin. Gas composition and carbon and hydrogen isotopic data suggest mostly thermogenic origin of coalbed gas in coals from Webster and Union Counties, Kentucky, in contrast to the dominantly biogenic character of coalbed gas in Ohio County, Kentucky.

  13. The influence of metal- and N-species addition in mesoporous carbons on the hydrogen adsorption capacity

    Energy Technology Data Exchange (ETDEWEB)

    Cai, J. [Université Lyon 1, CNRS UMR5256, Institut de Recherches sur la Catalyse et l' Environnement de Lyon, 2 Av. Einstein, 69626 Villeurbanne (France); Bennici, S., E-mail: simona.bennici@ircelyon.univ-lyon1.fr [Université Lyon 1, CNRS UMR5256, Institut de Recherches sur la Catalyse et l' Environnement de Lyon, 2 Av. Einstein, 69626 Villeurbanne (France); Shen, J. [Laboratory of Mesoscopic Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093 (China); Auroux, A. [Université Lyon 1, CNRS UMR5256, Institut de Recherches sur la Catalyse et l' Environnement de Lyon, 2 Av. Einstein, 69626 Villeurbanne (France)

    2015-07-01

    Mesoporous carbon (MC) and two types of N-containing mesoporous carbons (N-MC and C{sub 3}N{sub 4}-MC) were prepared from cost-effective materials and used for hydrogen storage both at 77 K and room temperature (RT). The mesoporous structure was confirmed by N{sub 2} adsorption isotherm at 77 K, and the characterization of the bulk and surface properties performed by ICP analysis, TEM, XRD, and XPS. The maximum hydrogen uptakes were found on N-MC (1.1 wt% of hydrogen) at 100 bar and RT and on MC (3.07 wt% of hydrogen) at 40 bar and 77 K. Pt, Pd, and Ru noble-metal were also added to the three carbon based supports in order to verify the existence of any spillover effect due to the metals presence and evaluate the influence on hydrogen storage capacity. - Highlights: • Biomass derived mesoporous carbons were modified by N and noble metal addition. • N atoms enhance the H{sub 2} adsorption capacity of mesoporous carbon at room temperature. • Ru/N-MC reaches the maximum theoretical limit of H{sub 2} storage for carbon materials.

  14. Zeolite Y Adsorbents with High Vapor Uptake Capacity and Robust Cycling Stability for Potential Applications in Advanced Adsorption Heat Pumps.

    Science.gov (United States)

    Li, Xiansen; Narayanan, Shankar; Michaelis, Vladimir K; Ong, Ta-Chung; Keeler, Eric G; Kim, Hyunho; McKay, Ian S; Griffin, Robert G; Wang, Evelyn N

    2015-01-01

    Modular and compact adsorption heat pumps (AHPs) promise an energy-efficient alternative to conventional vapor compression based heating, ventilation and air conditioning systems. A key element in the advancement of AHPs is the development of adsorbents with high uptake capacity, fast intracrystalline diffusivity and durable hydrothermal stability. Herein, the ion exchange of NaY zeolites with ingoing Mg(2+) ions is systematically studied to maximize the ion exchange degree (IED) for improved sorption performance. It is found that beyond an ion exchange threshold of 64.1%, deeper ion exchange does not benefit water uptake capacity or characteristic adsorption energy, but does enhance the vapor diffusivity. In addition to using water as an adsorbate, the uptake properties of Mg,Na-Y zeolites were investigated using 20 wt.% MeOH aqueous solution as a novel anti-freeze adsorbate, revealing that the MeOH additive has an insignificant influence on the overall sorption performance. We also demonstrated that the labscale synthetic scalability is robust, and that the tailored zeolites scarcely suffer from hydrothermal stability even after successive 108-fold adsorption/desorption cycles. The samples were analyzed using N2 sorption, (27)Al/(29)Si MAS NMR spectroscopy, ICP-AES, dynamic vapor sorption, SEM, Fick's 2(nd) law and D-R equation regressions. Among these, close examination of sorption isotherms for H2O and N2 adsorbates allows us to decouple and extract some insightful information underlying the complex water uptake phenomena. This work shows the promising performance of our modified zeolites that can be integrated into various AHP designs for buildings, electronics, and transportation applications.

  15. Zeolite Y adsorbents with high vapor uptake capacity and robust cycling stability for potential applications in advanced adsorption heat pumps

    Energy Technology Data Exchange (ETDEWEB)

    Li, XS; Narayanan, S; Michaelis, VK; Ong, TC; Keeler, EG; Kim, H; Mckay, IS; Griffin, RG; Wang, EN

    2015-01-01

    Modular and compact adsorption heat pumps (AHPs) promise an energy-efficient alternative to conventional vapor compression based heating, ventilation and air conditioning systems. A key element in the advancement of AHPs is the development of adsorbents with high uptake capacity, fast intracrystalline diffusivity and durable hydrothermal stability. Herein, the ion exchange of NaY zeolites with ingoing Mg2+ ions is systematically studied to maximize the ion exchange degree (IED) for improved sorption performance. It is found that beyond an ion exchange threshold of 64.1%, deeper ion exchange does not benefit water uptake capacity or characteristic adsorption energy, but does enhance the vapor diffusivity. In addition to using water as an adsorbate, the uptake properties of Mg, Na-Y zeolites were investigated using 20 wt.% MeOH aqueous solution as a novel anti-freeze adsorbate, revealing that the MeOH additive has an insignificant influence on the overall sorption performance. We also demonstrated that the lab-scale synthetic scalability is robust, and that the tailored zeolites scarcely suffer from hydrothermal stability even after successive 108-fold adsorption/desorption cycles. The samples were analyzed using N-2 sorption, Al-27/Si-29 MAS NMR spectroscopy, ICP-AES, dynamic vapor sorption, SEM, Fick's 2nd law and D-R equation regressions. Among these, close examination of sorption isotherms for H2O and N-2 adsorbates allows us to decouple and extract some insightful information underlying the complex water uptake phenomena. This work shows the promising performance of our modified zeolites that can be integrated into various AHP designs for buildings, electronics, and transportation applications. (C) 2014 Elsevier Inc. All rights reserved.

  16. Fate and aqueous transport of mercury in light of the Clean Air Mercury Rule for coal-fired electric power plants

    Science.gov (United States)

    Arzuman, Anry

    Mercury is a hazardous air pollutant emitted to the atmosphere in large amounts. Mercury emissions from electric power generation sources were estimated to be 48 metric tons/year, constituting the single largest anthropogenic source of mercury in the U.S. Settled mercury species are highly toxic contaminants of the environment. The newly issued Federal Clean Air Mercury Rule requires that the electric power plants firing coal meet the new Maximum Achievable Mercury Control Technology limit by 2018. This signifies that all of the air-phase mercury will be concentrated in solid phase which, based on the current state of the Air Pollution Control Technology, will be fly ash. Fly ash is utilized by different industries including construction industry in concrete, its products, road bases, structural fills, monifills, for solidification, stabilization, etc. Since the increase in coal combustion in the U.S. (1.6 percent/year) is much higher than the fly ash demand, large amounts of fly ash containing mercury and other trace elements are expected to accumulate in the next decades. The amount of mercury transferred from one phase to another is not a linear function of coal combustion or ash production, depends on the future states of technology, and is unknown. The amount of aqueous mercury as a function of the future removal, mercury speciation, and coal and aquifer characteristics is also unknown. This paper makes a first attempt to relate mercury concentrations in coal, flue gas, fly ash, and fly ash leachate using a single algorithm. Mercury concentrations in all phases were examined and phase transformation algorithms were derived in a form suitable for probabilistic analyses. Such important parameters used in the transformation algorithms as Soil Cation Exchange Capacity for mercury, soil mercury selectivity sequence, mercury activity coefficient, mercury retardation factor, mercury species soil adsorption ratio, and mercury Freundlich soil adsorption isotherm

  17. Biochar characteristics produced from food-processing products and their sorptive capacity for mercury and phenanthrene

    Science.gov (United States)

    Fotopoulou, Kalliopi N.; Karapanagioti, Hrissi K.; Manariotis, Ioannis D.

    2015-04-01

    Various organic-rich wastes including wood chips, animal manure, and crop residues have been used for biochar production. Biochar is used as an additive to soils to sequester carbon and improve soil fertility but its use as a sorbent for environmental remediation processes is gaining increased attention. Surface properties such as point of zero charge, surface area and pore volume, surface topography, surface functional groups and acid-base behavior are important factors, which affect sorption efficiency. Understanding the surface alteration of biochars increases our understanding of the pollutant-sorbent interaction. The scope of the present work was to evaluate the effect of key characteristics of biochars on their sorptive properties. Raw materials for biochar production were evaluated including byproducts from brewering, coffee, wine, and olive oil industry. The charring process was performed at different temperatures under limited-oxygen conditions using specialized containers. The surface area, the pore volume, and the average pore size of the biochars were determined. Open surface area and micropore volume were determined using t-plot method and Harkins & Jura equation. Raw food-processing waste demonstrates low surface area that increases by 1 order of magnitude by thermal treatment up to 750oC. At temperatures from 750 up to 900oC, pyrolysis results to biochars with surface areas 210-700 m2/g. For the same temperature range, a high percentage (46 to73%) of the pore volume of the biochars is due to micropores. Positive results were obtained when high surface area biochars were tested for their ability to remove organic (i.e. phenanthrene) and inorganic (i.e. mercury) compounds from aqueous solutions. All these properties point to new materials that can effectively be used for environmental remediation.

  18. High surface-area amidoxime-based polymer fibers co-grafted with various acid monomers yielding increased adsorption capacity for the extraction of uranium from seawater.

    Science.gov (United States)

    Oyola, Yatsandra; Dai, Sheng

    2016-06-01

    Uranium is dissolved in the ocean at a uniform concentration of 3.34 ppb, which translates to approximately 4-5 billion tons of uranium. The development of adsorbents that can extract uranium from seawater has been a long term goal, but the extremely dilute uranium concentration along with the competition of other metal salts (which are at higher concentrations) has hindered the development of an economical adsorption process. Several acid monomers were co-grafted with acrylonitrile (AN) to help increase the hydrophilicity of the adsorbent to improve access to the metal adsorption sites. Grafting various acid monomers on PE fibers was found to significantly affect the uranium adsorption in simulated seawater in the following order: acrylic acid (AA) uranium adsorption capacity significantly increased when Mohr's salt was added with acrylic acid, most likely due to the reduction of co-polymerization of the monomers. When testing under more realistic conditions, the acid-grafted PE fiber adsorbents were exposed to natural seawater (more dilute uranium), the uranium adsorption capacity increased in the following order: MAA uranium adsorption capacity with each acid monomer was related to higher grafting of AN and therefore a higher conversion to amidoxime (AO). PMID:27145863

  19. Removal of mercury from flue gas using Ca-based sorbents

    Energy Technology Data Exchange (ETDEWEB)

    Ren, J.L.; Luo, Y.Y.; Xu, Z.; Zhong, Y.J. [Zhejiang Univ. of Technology, Hangzhou (China). MOE Key Laboratory of Mechanical Manufacture and Automation; Zhou, J.S. [Zhejiang Univ., Hangzhou, (China). Inst. of Thermal Power Engineering, State Key Laboratory of Clean Energy Utilization

    2008-07-01

    Mercury (Hg) emissions from power plants raise environmental concerns, particularly in China's coal-fired power plants. Mercury is present mainly in the vapor form (Hg0) and cannot be captured effectively by existing particulate removal systems because of its high volatility and insolubility in water. It is therefore necessary to design and manufacture more cost-effective mercury sorbents to replace conventional sorbents already in use for mercury control. This paper reported on a study in which the characteristics of mercury sorption by 3 kinds of calcium (Ca)based sorbents were studied, notably lime, hydrated lime and a mixture of fly ash and hydrated lime (MFC). Adsorption experiments were performed in a bench-scale fixed-bed mercury sorption facility with a mercury permeation tube embedded in an isothermal water bath and simulated flue gas compositions. The effects of sulphur dioxide (SO{sub 2}) on adsorption were investigated along with the adsorption mechanism. The study showed that the performance of Ca-based sorbents was better in the presence of SO{sub 2} than the baseline conditions. In the absence SO{sub 2}, the Hg0 adsorption effectiveness of the 3 kinds of Ca-based sorbents was lower. In the presence of SO{sub 2}, adsorption efficiency improved by 15 to 20 per cent and the adsorption capacity was more than 50 per cent at 30 minutes of exposure of sorbents to the flue gas. Higher temperature was found to be beneficial to the adsorption process. SO{sub 2} reacted with the Ca-based sorbents and produced active adsorption sites on the surface of the sorbents, thus oxidating Hg0 to Hg2+ and improving capture efficiency by chemisorption. 14 refs., 2 tabs., 8 figs.

  20. Dose-dependent adsorptive capacity of activated charcoal for gastrointestinal decontamination of a simulated paracetamol overdose in human volunteers

    DEFF Research Database (Denmark)

    Gude, Anne-Bolette Jill; Hoegberg, Lotte Christine Groth; Riis Angelo, Helle;

    2010-01-01

    The amount of activated charcoal needed to treat drug overdoses has arbitrarily been set at a charcoal-drug ratio of 10:1. Recent in vitro studies have shown a larger adsorptive capacity for activated charcoal when used in a model of paracetamol overdose. In the present study, we investigated...... to be of similar size compared to the control, although statistics were weak. The AUC of the 5-g dose was 59% larger than the AUC of the 50-g dose (p = 0.0003). The terminal elimination half-life (t(1/2)) of paracetamol was 1.6 (CI 1.4-2.0) and 1.9 (CI 1.5-2.4) hr for 50 and 25 g, respectively (NS), and 2.5 (CI 1...

  1. Modification of cyanobacterial bloom-derived biomass using potassium permanganate enhanced the removal of microcystins and adsorption capacity toward cadmium (II)

    Energy Technology Data Exchange (ETDEWEB)

    Shao, Jihai [College of Resources and Environment, Hunan Agricultural University, Changsha 410128 (China); Hunan Provincial Key Laboratory of Farmland Pollution Control and Agricultural Resources Use, Hunan Agricultural University, Changsha 410128 (China); Gu, Ji-Dong [Hunan Provincial Key Laboratory of Farmland Pollution Control and Agricultural Resources Use, Hunan Agricultural University, Changsha 410128 (China); Laboratory of Environmental Microbiology and Toxicology, School of Biological Sciences, The University of Hong Kong, Hong Kong Special Administrative Region (Hong Kong); Peng, Liang; Luo, Si; Luo, Huili [College of Resources and Environment, Hunan Agricultural University, Changsha 410128 (China); Yan, Zhiyong, E-mail: zhyyan111@163.com [College of Resources and Environment, Hunan Agricultural University, Changsha 410128 (China); Wu, Genyi, E-mail: wugenyi99@163.com [College of Resources and Environment, Hunan Agricultural University, Changsha 410128 (China)

    2014-05-01

    Highlights: • Potassium permanganate removed microcystins in the cyanobacterial bloom-derived biomass (CBDB). • Potassium permanganate oxidation caused the transformation of hydroxyl to carboxyl on the CBDB. • Manganese dioxide was formed on the surface of CBDB. • Potassium permanganate oxidation process increased the adsorption capacity of CBDB toward Cd(II). - Abstract: Cyanobacterial biomass shows high adsorption capacity toward heavy metal ions. However, the cyanotoxins in the cyanobacterial biomass inhibit its application in heavy metals removal. In order to safely and effectively remove Cd(II) from water using cyanobacterial bloom-derived biomass (CBDB), KMnO{sub 4} was used to modify CBDB. The results indicated that the microcystins in the CBDB were successfully removed by KMnO{sub 4}. Potassium permanganate oxidation caused the transformation of hydroxyl to carboxyl on the CBDB, and formed manganese dioxide on the surface of CBDB. The oxidized CBDB showed higher adsorption capacity toward Cd(II) than that of unoxidized treatment. The optimal KMnO{sub 4} concentration for increasing the adsorption capacity of CBDB toward Cd(II) was 0.2 g/L. The adsorption isotherm of Cd(II) by oxidized- or unoxidized-CBDB was well fitted by Langmuir model, indicating that the adsorption of Cd(II) by CBDB was monolayer adsorption. The desorption ratio of Cd(II) from oxidized CBDB was higher than that from unoxidized CBDB in the desorption process using NH{sub 4}NO{sub 3} and EDTA as desorbent. The results presented in this study suggest that KMnO{sub 4} modified CBDB may be used as a safe and high efficient adsorbent in Cd(II) removal from water.

  2. 活性焦汞吸附特性及动力学机理分析%Performance and kinetics of mercury adsorption over Tai-Xi activated coke

    Institute of Scientific and Technical Information of China (English)

    张海茹; 吴昊; 刘浩; 王萌; 杨宏旻

    2013-01-01

    通过固态吸附剂汞吸附效能测定系统进行了太西活性焦吸附单质汞的实验,考察单质汞Hg0入口浓度和温度对太西活性焦脱汞性能的影响并探讨了吸附机理.结果表明:在CO2/N2/O2/NO/Hg0体系中,不同Hg0入口浓度获得的汞脱除效率曲线相似,脱除效率随Hg0入口浓度增大而增加;变入口浓度工况下,汞的吸附全过程遵循准二级动力学反应模型,该吸附过程以化学吸附为主;在反应温度从403 K升高到423 K的过程中,系统发生了化学吸附或者化学反应,423 K可作为活性焦的最佳除汞温度;Bangham方程可对变温工况下活性焦脱除单质汞的吸附过程进行准确描述,并获得不同温度下活性焦脱汞的吸附速率常数存在k423K> k463K >k403K的关系.%The tests of mercury adsorption on Tai-Xi activated coke were conducted in an adsorption system of fixed-bed reactor. The effect of inlet mercury concentration and temperature on adsorption efficiency (removal of mercury) was studied using a simulated flue gas that was prepared by mixing flue gas component CO2, N2, O2, NO and Hg0 vapors came from a permeation tube. The results show that there is similar shape of adsorption curve for different initial mercury concentrations and efficiency of mercury removal increases with increase of inlet mercury concentration. The initial port of breakthrough curve shows that the adsorption rate is rapid, then slow and slow until to adsorption saturation. The uptake process of mercury by activated coke can be well fitted by a pseudo-second order kinetics model, indicating that for CO2/N2/O2/NO/Hg0 system, the adsorption of mercury on the activated coke takes mainly place by chemical adsorption or chemical reaction. The optimal temperature is 423 K for the best mercury removal. The Bangham equation can be applied to describe the adsorption behavior at different operation temperature, and the adsorption rate constants at different temperature follow

  3. Effect of carbonation temperature on CO2 adsorption capacity of CaO derived from micro/nanostructured aragonite CaCO3

    Science.gov (United States)

    Hlaing, Nwe Ni; Sreekantan, Srimala; Hinode, Hirofumi; Kurniawan, Winarto; Thant, Aye Aye; Othman, Radzali; Mohamed, Abdul Rahman; Salime, Chris

    2016-07-01

    Recent years, CaO-based synthetic materials have been attracted attention as potential adsorbents for CO2 capture mainly due to their high CO2 adsorption capacity. In this study, micro/nanostructured aragonite CaCO3 was synthesized by a simple hydrothermal method with using polyacrylamide (PAM). The structural, morphological and thermal properties of the synthesized sample were investigated by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM) and thermogravimetry analysis (TG-DTA). The XRD and FESEM results showed that the obtained sample was aragonite CaCO3 with aggregated nanorods and microspheres composed of nanorods. A TG-DTA apparatus with Thermoplus 2 software was used to investigate the effect of carbonation temperature on the CO2 adsorption capacity of CaO derived from aragonite CaCO3 sample. At 300 °C, the sample reached the CO2 adsorption capacity of 0.098 g-CO2/g-adsorbent, whereas the sample achieved the highest capacity of 0.682 g-CO2/g-adsorbent at 700 °C. The results showed that the carbonation temperature significantly influenced on the CO2 adsorption capacity of the CaO derived from aragonite CaCO3.

  4. Effects of Mn, Cu doping concentration to the properties of magnetic nanoparticles and arsenic adsorption capacity in wastewater

    Energy Technology Data Exchange (ETDEWEB)

    Thi, Tran Minh, E-mail: tranminhthi@hnue.edu.vn; Trang, Nguyen Thi Huyen; Van Anh, Nguyen Thi

    2015-06-15

    Highlights: • Investigation the decrease of saturate magnetic moment of Fe{sub 3}O{sub 4} over time. • Substitution of Mn, Cu ions into Fe position to create stable properties of materials. • Investigate the surface and mesopore structure of nanoparticles. • The arsenic adsorption capacity of Cu doped Fe{sub 3}O{sub 4} nanomaterials is higher than of Fe{sub 3}O{sub 4} and Mn doped Fe{sub 3}O{sub 4} nanomaterials. - Abstract: The research results of Fe{sub 3}O{sub 4} and Mn, Cu doped Fe{sub 3}O{sub 4} nanomaterials synthesized by a chemical method for As(III) wastewater treatment are presented in this paper. The X-ray diffraction patterns and transmission electron microscopy images showed that samples had the cubic spinel structure with the grain sizes were varied from 9.4 nm to 18.1 nm. The results of vibrating sample magnetometer measurements at room temperature showed that saturation magnetic moments of Fe{sub 1−x}Cu{sub x}Fe{sub 2}O{sub 4} and Fe{sub 1−x}Mn{sub x}Fe{sub 2}O{sub 4} samples decreased from 65.9 emu/g to 53.2 emu/g and 65.9 emu/g to 61.5 emu/g, respectively, with the increase of Cu, Mn concentrations from 0.0 to 0.15. The nitrogen adsorption–desorption isotherm of a typical Fe{sub 3}O{sub 4} sample at 77 K was studied in order to investigate the surface and porous structure of nanoparticles by BET method. The specific surface area of Fe{sub 3}O{sub 4} magnetic nanoparticles was calculated about of 100.2 m{sup 2}/g. The pore size distribution of about 15–20 nm calculated by the BJH (Barrett, Joyner, and Halendar) method at a relative pressure P/P{sub 0} of about 1. Although the saturation magnetic moments of samples decreased when the increase of doping concentration, but the arsenic adsorption capacity of Cu doped Fe{sub 3}O{sub 4} nanoparticles is better than that of Fe{sub 3}O{sub 4} and Mn doped Fe{sub 3}O{sub 4} nanoparticles in a solution with pH = 7. In the solution with a pH > 14, the arsenic adsorption of magnetic

  5. Estimating prion adsorption capacity of soil by BioAssay of Subtracted Infectivity from Complex Solutions (BASICS.

    Directory of Open Access Journals (Sweden)

    A Christy Wyckoff

    Full Text Available Prions, the infectious agent of scrapie, chronic wasting disease and other transmissible spongiform encephalopathies, are misfolded proteins that are highly stable and resistant to degradation. Prions are known to associate with clay and other soil components, enhancing their persistence and surprisingly, transmissibility. Currently, few detection and quantification methods exist for prions in soil, hindering an understanding of prion persistence and infectivity in the environment. Variability in apparent infectious titers of prions when bound to soil has complicated attempts to quantify the binding capacity of soil for prion infectivity. Here, we quantify the prion adsorption capacity of whole, sandy loam soil (SLS typically found in CWD endemic areas in Colorado; and purified montmorillonite clay (Mte, previously shown to bind prions, by BioAssay of Subtracted Infectivity in Complex Solutions (BASICS. We incubated prion positive 10% brain homogenate from terminally sick mice infected with the Rocky Mountain Lab strain of mouse-adapted prions (RML with 10% SLS or Mte. After 24 hours samples were centrifuged five minutes at 200 × g and soil-free supernatant was intracerebrally inoculated into prion susceptible indicator mice. We used the number of days post inoculation to clinical disease to calculate the infectious titer remaining in the supernatant, which we subtracted from the starting titer to determine the infectious prion binding capacity of SLS and Mte. BASICS indicated SLS bound and removed ≥ 95% of infectivity. Mte bound and removed lethal doses (99.98% of prions from inocula, effectively preventing disease in the mice. Our data reveal significant prion-binding capacity of soil and the utility of BASICS to estimate prion loads and investigate persistence and decomposition in the environment. Additionally, since Mte successfully rescued the mice from prion disease, Mte might be used for remediation and decontamination protocols.

  6. Effect of oxygen potential on sulphur dioxide activation of oil sands fluid coke and characteristics of activated coke in mercury adsorption

    Energy Technology Data Exchange (ETDEWEB)

    Morris, E.A.; Jia, C.Q. [Toronto Univ., ON (Canada). Dept. of Chemical Engineering and Applied Chemistry; Tong, S. [Wuhan Univ. of Science and Technology, Wuhan, Hobei (China). Dept. of Chemical Engineering

    2007-07-01

    A sulphur-impregnated activated carbon (SIAC) technology was modified for use in copper smelters in order to mitigate mercury and sulphur dioxide (SO{sub 2}) emissions. Elemental sulphur was captured as a co-product. The study examined the feasibility of reducing levels of SO{sub 2} using fluid coke in the copper smelter flue. SIAC properties were optimized in order to capture vapour phase mercury. Raw fluid coke samples were used to measure SO{sub 2} flow rates. Gas composition was varied to mimic concentrations found during normal operation of copper converters. Gas chromatography was used to analyze reactions products and to prove the hypothesis that mercury capacity is influenced by the oxygen potential of the activation gas due to changes in surface sulphur types developed from reduced sulphur species. Results of the study showed that oxygen levels at 5 per cent did not play a significant role in pore development. It was concluded that increased residence times contributed to reductions in SO{sub 2} and elemental S yields. 13 refs., 1 tab., 7 figs.

  7. High adsorption capacity of two Zn-based metal-organic frameworks by ultrasound assisted synthesis.

    Science.gov (United States)

    Masoomi, Mohammad Yaser; Bagheri, Minoo; Morsali, Ali

    2016-11-01

    Micro- and nano-rods and plates of two 3D, porous Zn(II)-based metal-organic frameworks [Zn(oba)(4-bpdh)0.5]n·(DMF)1.5 (TMU-5) and [Zn(oba)(4-bpmb)0.5]n (DMF)1.5 (TMU-6) were prepared by sonochemical process and characterized by scanning electron microscopy, X-ray powder diffraction and IR spectroscopy. These MOFs were synthesized using a non-linear dicarboxylate (H2oba=4,4-oxybisbenzoic acid) and two linear N-donor (4-bpdh=2,5-bis(4-pyridyl)-3,4-diaza-2,4-hexadiene and 4-bpmb=N(1),N(4)-bis((pyridin-4-yl)methylene)benzene-1,4-diamine) ligands by ultrasonic irradiation. Sonication time and concentration of initial reagents influencing size and morphology of nano-structured MOFs, were also studied. Calcination of TMU-5 and TMU-6 at 550°C under air atmosphere yields ZnO nanoparticles. TMU-5 and TMU-6 exhibited maximum percent adsorption of 96.2% and 92.8% of 100ppm rhodamine B dye, respectively, which obeys first order reaction kinetics.

  8. Novel regenerable sorbent based on Zr-Mn binary metal oxides for flue gas mercury retention and recovery.

    Science.gov (United States)

    Xie, Jiangkun; Qu, Zan; Yan, Naiqiang; Yang, Shijian; Chen, Wanmiao; Hu, Lingang; Huang, Wenjun; Liu, Ping

    2013-10-15

    To capture and recover mercury from coal-fired flue gas, a series of novel regenerable sorbents based on Zr-Mn binary metal oxides were prepared and employed at a relatively low temperature. PXRD, TEM, TPR, XPS, and N2-adsorption methods were employed to characterize the sorbents. The Hg(0) adsorption performance of the sorbents was tested, and the effects of the main operation parameters and the gas components on the adsorption were investigated. Zr significantly improved the sorbent's mercury capacity, which was nearly 5mg/g for Zr0.5Mn0.5Oy. Furthermore, the spent sorbent could be regenerated by heating to 350°C, and the highly concentrated elemental mercury released could be facilely recycled. Therefore, a much greener process for mercury capture and recovery could be anticipated based on this regenerable sorbent. PMID:23933289

  9. The effect of low-NOx combustion on residual carbon in fly ash and its adsorption capacity for air entrainment admixtures in concrete

    DEFF Research Database (Denmark)

    Pedersen, Kim Hougaard; Jensen, Anker Degn; Dam-Johansen, Kim

    2010-01-01

    Fly ash from pulverized coal combustion contains residual carbon that can adsorb the air-entraining admixtures (AEAs) added to control the air entrainment in concrete. This is a problem that has increased by the implementation of low-NOx combustion technologies. In this work, pulverized fuel has...... by up to a factor of 25. This was due to a lower carbon content in the ash and a lower specific AEA adsorptivity of the carbon. The latter was suggested to be caused by changes in the adsorption properties of the unburned char and a decreased formation of soot, which was found to have a large AEA...... adsorption capacity based on measurements on a carbon black. The NOx formation increased by up to three times with more oxidizing conditions and thus, there was a trade-off between the AEA requirements of the ash and NOx formation. The type of fuel had high impact on the AEA adsorption behavior of the ash...

  10. CO2 Adsorption in Low-Rank Coals: Progress Toward Assessing the National Capacity to Store CO2 in the Subsurface

    Science.gov (United States)

    Stanton, R. W.; Burruss, R. C.; Flores, R. M.; Warwick, P. D.

    2001-05-01

    Subsurface environments for geologic storage of CO2 from combustion of fossil fuel include saline formations, depleted oil and gas reservoirs, and unmineable coalbeds. Of these environments, storage in petroleum reservoirs and coal beds offers a potential economic benefit of enhanced recovery of energy resources. Meaningful assessment of the volume and geographic distribution of storage sites requires quantitative estimates of geologic factors that control storage capacity. The factors that control the storage capacity of unmineable coalbeds are poorly understood. In preparation for a USGS assessment of CO2 storage capacity we have begun new measurements of CO2 and CH4 adsorption isotherms of low-rank coal samples from 4 basins. Initial results for 13 samples of low-rank coal beds from the Powder River Basin (9 subbituminous coals), Greater Green River Basin (1 subbituminous coal), Williston Basin (2 lignites) and the Gulf Coast (1 lignite) indicate that their adsorption capacity is up to 10 times higher than it is for CH4. These values contrast with published measurements of the CO2 adsorption capacity of bituminous coals from the Fruitland Formation, San Juan basin, and Gates Formation, British Columbia, that indicate about twice as much carbon dioxide as methane can be adsorbed on coals. Because CH4 adsorption isotherms are commonly measured on coals, CO2 adsorption capacity can be estimated if thecorrect relationship between the gases is known. However, use a factor to predict CO2 adsorption that is twice that of CH4 adsorption, which is common in the published literature, grossly underestimates the storage capacity of widely distributed, thick low-rank coal beds. Complete petrographic and chemical characterization of these low-rank coal samples is in progress. Significant variations in adsorption measurements among samples are depicted depending on the reporting basis used. Properties were measured on an "as received" (moist) basis but can be converted to a

  11. Functionalized diatom silica microparticles for removal of mercury ions

    Directory of Open Access Journals (Sweden)

    Yang Yu, Jonas Addai-Mensah and Dusan Losic

    2012-01-01

    Full Text Available Diatom silica microparticles were chemically modified with self-assembled monolayers of 3-mercaptopropyl-trimethoxysilane (MPTMS, 3-aminopropyl-trimethoxysilane (APTES and n-(2-aminoethyl-3-aminopropyl-trimethoxysilane (AEAPTMS, and their application for the adsorption of mercury ions (Hg(II is demonstrated. Fourier transform infrared spectroscopy and x-ray photoelectron spectroscopy analyses revealed that the functional groups (–SH or –NH2 were successfully grafted onto the diatom silica surface. The kinetics and efficiency of Hg(II adsorption were markedly improved by the chemical functionalization of diatom microparticles. The relationship among the type of functional groups, pH and adsorption efficiency of mercury ions was established. The Hg(II adsorption reached equilibrium within 60 min with maximum adsorption capacities of 185.2, 131.7 and 169.5 mg g-1 for particles functionalized with MPTMS, APTES and AEAPTMS, respectively. The adsorption behavior followed a pseudo-second-order reaction model and Langmuirian isotherm. These results show that mercapto- or amino-functionalized diatom microparticles are promising natural, cost-effective and environmentally benign adsorbents suitable for the removal of mercury ions from aqueous solutions.

  12. SILICA GEL WITH COVALENTLY IMMOBILIZED THIOSEMICARBAZIDE FOR SOLID-PHASE CONCENTRATION OF MERCURY

    OpenAIRE

    Konshina, Dzh. N.; Open'ko, V. V.; Temerdashev, Z. A.; Konshin, V. V.; Romanovskii, K. A.

    2014-01-01

    А new thiosemicarbazide modified silica gel sorbent was prepared and applied for preconcentration of trace mercury(II) prior to the measurement by spectrophotometry and atomic absorption spectroscopy. The optimization of some analytical parameters affecting the adsorption of the analyte such as acidity, shaking time, sample flow rate and volume, eluent condition, and interfering substances were investigated. At pH 2, the maximum static adsorption capacity of Hg(II) onto the thiosemicarbazide ...

  13. 褐煤活性焦烟气脱汞的实验研究%Mercury removal from flue gas by lignite activated coke

    Institute of Scientific and Technical Information of China (English)

    白中华; 史亚微; 张旭辉; 杨文辉; 张向洲; 石长江; 赵玉冰

    2014-01-01

    Coal-fired power plant mercury pollution has attracted a growing concern, now the current mercury removal method which has an application prospect is the adsorption of mercury removal, and therefore the development of cost-effective mercury removal sorbent been studied extensively. An experiment was conducted to study the effects of lignite activated coke on the mercury adsorption using a bench-scale fixed bed,including the inlet concentration of mercury pollutants,the quality of adsorbent,the composition of flue gas and the type of adsorbent and so on.The results show that the lignite activated coke has some adsorption capacity for mercury in flue gas,the activated coke adsorption rate increases with the increase of entrance mercury concentration and the quality of activated coke.The SO2,NO in flue gas can improve mercury adsorption capacity of activated coke.Although the mercury adsorption capacity of activated coke is lower than activated carbon with S solution and activated carbon only for mercury adsorption,the improvement of activation way of activated coke can enhance the performance of its mercury adsorption.%燃煤电厂汞污染越来越受到关注,目前具有应用前景的脱汞方法为吸附脱汞,因此研发高效低成本的脱汞吸附剂被广泛研究。在搭建的固定床吸附反应系统上对自制的褐煤活性焦脱汞性能进行了实验研究,研究了汞污染物的入口浓度,吸附剂的量、烟气成分及吸附剂的种类对吸附汞的影响。结果表明:活性焦吸附剂对烟气中的气态汞均有一定的吸附能力,其吸附效果随着入口汞浓度和吸附剂量的增加而增加;烟气中的SO2、NO气体对活性焦吸附汞有一定的促进作用。活性焦脱汞效率与载硫活性炭、脱汞专用活性炭相比还存在一定差距,但可通过改进活性焦的活化方式提高脱汞性能。

  14. Direct observation of solid-phase adsorbate concentration profile in powdered activated carbon particle to elucidate mechanism of high adsorption capacity on super-powdered activated carbon.

    Science.gov (United States)

    Ando, Naoya; Matsui, Yoshihiko; Matsushita, Taku; Ohno, Koichi

    2011-01-01

    Decreasing the particle size of powdered activated carbon (PAC) by pulverization increases its adsorption capacities for natural organic matter (NOM) and polystyrene sulfonate (PSS, which is used as a model adsorbate). A shell adsorption mechanism in which NOM and PSS molecules do not completely penetrate the adsorbent particle and instead preferentially adsorb near the outer surface of the particle has been proposed as an explanation for this adsorption capacity increase. In this report, we present direct evidence to support the shell adsorption mechanism. PAC particles containing adsorbed PSS were sectioned with a focused ion beam, and the solid-phase PSS concentration profiles of the particle cross-sections were directly observed by means of field emission-scanning electron microscopy/energy-dispersive X-ray spectrometry (FE-SEM/EDXS). X-ray emission from sulfur, an index of PSS concentration, was higher in the shell region than in the inner region of the particles. The X-ray emission profile observed by EDXS did not agree completely with the solid-phase PSS concentration profile predicted by shell adsorption model analysis of the PSS isotherm data, but the observed and predicted profiles were not inconsistent when the analytical errors were considered. These EDXS results provide the first direct evidence that PSS is adsorbed mainly in the vicinity of the external surface of the PAC particles, and thus the results support the proposition that the increase in NOM and PSS adsorption capacity with decreasing particle size is due to the increase in external surface area on which the molecules can be adsorbed. PMID:20851447

  15. Investigation of SO{sub 2} adsorption capacity of the activated carbon with O{sub 2}-NH{sub 3} treatment

    Energy Technology Data Exchange (ETDEWEB)

    Ko, Yoon Hee; Seo, Kyung Won [Ajou University, Suwon (Korea, Republic of); Park, Dal Keun [KIST, Seoul (Korea, Republic of)

    1995-05-01

    Activated carbons, modified by oxygen and ammonia treatment, were tested for their catalytic activity in the SO{sub 2} adsorption. The modified activated carbons showed higher SO{sub 2} adsorption capacity compared with the untreated activated carbons. In this study the surface of activated carbon was modified to introduce the surface oxygen and nitrogen functional groups from NH{sub 3} and/or O{sub 2} treatment. In this experiment the conditions of modification varied with the NH{sub 3} concentrations(0{approx}25 vol%) and temperature (473{approx}1273 K) of the furnace, which directly affect surface functionalities, elemental composition, surface area and pore structure. The adsorption capacities were measured in an electric torsion balance(Cahn 2000). The activated carbons were characterized by temperature programmed desorption(TPD), Fourier transform infrared spectroscopy(FTIR), and acid-base titration. The maximum capacity of SO{sub 2} adsorption of the carbon sample(SO{sub 2} mg/m{sup 2} surface area) was obtained in the temperature range of 973{approx}1173 K. The activated carbons, treated with NH{sub 3}(up to 25% with O{sub 2} 3% of fixed amount), adsorbed SO{sub 2} about 48% more than the untreated activated carbons. (author). 9 refs., 11 figs., 1 tab.

  16. Synthesis and granulation of a titanosilicate with adsorption capacity for Cs to be used for treating de ILLW of the Ezeiza Radioisotope Production Plant

    International Nuclear Information System (INIS)

    The sitinakite structured titanosilicate is widely used for treating ILLW thanks to its capacity for adsorbing both Cs-137 and Sr-90. Its effectiveness lies in its incredibly high selectivity for such radioisotopes, which makes it useful in complex isotope solutions and even in strong acid and alkaline conditions. In Argentina, an off-the-shelve titanosilicate was used in Ezeiza's radioisotope production plant. Because of commercial restrictions, it is no longer available so an inhouse production is being developed. The aim of this project consists of the following: 1. Synthesis of titanosilicate and structural characterization 2. Adsorption kinetics of Cs+ 3. Upscale of the synthesis process 4. Assessment of the influence of synthesis temperature and time on product crystallinity 5. Measurement of adsorption capacity of commercial titanosilicates IE910, IE911 and novel RC15H 6. Separative performance column essay and breakthrough plot 7. Chemical and radiolysis resistance of the adsorbent powder binder Polyacrylonitrile (PAN) in contact with the actual waste Throughout this work we have studied the optimum synthesis conditions capable of rendering a sitinakite structured titanosilicate, assessed its Cs+ adsorption kinetics, adsorption capacity, crystal phase and purity via DRX, particle size with Laser Light Scattering technique. We have also conducted column breakthrough experiments and tried the chemical and radiolysis resistance of the final product (author)

  17. Regenerative process for removal of mercury and other heavy metals from gases containing H.sub.2 and/or CO

    Science.gov (United States)

    Jadhav, Raja A.

    2009-07-07

    A method for removal of mercury from a gaseous stream containing the mercury, hydrogen and/or CO, and hydrogen sulfide and/or carbonyl sulfide in which a dispersed Cu-containing sorbent is contacted with the gaseous stream at a temperature in the range of about 25.degree. C. to about 300.degree. C. until the sorbent is spent. The spent sorbent is contacted with a desorbing gaseous stream at a temperature equal to or higher than the temperature at which the mercury adsorption is carried out, producing a regenerated sorbent and an exhaust gas comprising released mercury. The released mercury in the exhaust gas is captured using a high-capacity sorbent, such as sulfur-impregnated activated carbon, at a temperature less than about 100.degree. C. The regenerated sorbent may then be used to capture additional mercury from the mercury-containing gaseous stream.

  18. Effect of HNO{sub 3} treatment on the SO{sub 2} adsorption capacity of activated carbon prepared from Chinese low-rank coal

    Energy Technology Data Exchange (ETDEWEB)

    Hang Wenhui; Wang ling; Li Shurong [China Coal Research Institute, Beijing (China)

    1999-11-01

    SO{sub 2} removal from flue gas by activated carbon and HNO{sub 3} treated activated carbon from Chinese low-rank coal was studied. SO{sub 2} adsorption on activated carbon is mainly chemisorption. There was shown to be a correlation between adsorption capacity and the number of active sites on the carbon surface. HNO{sub 3} treatment transforms C-H bonds in activated carbon into active sites, for removal of SO{sub 2}. 2 figs., 2 tabs.

  19. LabVIEW-based sequential-injection analysis system for the determination of trace metals by square-wave anodic and adsorptive stripping voltammetry on mercury-film electrodes

    OpenAIRE

    Anastasios Economou; Anastasios Voulgaropoulos

    2003-01-01

    The development of a dedicated automated sequential-injection analysis apparatus for anodic stripping voltammetry (ASV) and adsorptive stripping voltammetry (AdSV) is reported. The instrument comprised a peristaltic pump, a multiposition selector valve and a home-made potentiostat and used a mercury-film electrode as the working electrodes in a thin-layer electrochemical detector. Programming of the experimental sequence was performed in LabVIEW 5.1. The sequence of operations included format...

  20. Enhanced capture of elemental mercury by bamboo-based sorbents

    Energy Technology Data Exchange (ETDEWEB)

    Tan, Zengqiang [State Key Laboratory of Coal Combustion, Huazhong University of Science and Technology, Wuhan, Hubei 430074 (China); Xiang, Jun, E-mail: xiangjun@mail.hust.edu.cn [State Key Laboratory of Coal Combustion, Huazhong University of Science and Technology, Wuhan, Hubei 430074 (China); Su, Sheng, E-mail: susheng_sklcc@hotmail.com [State Key Laboratory of Coal Combustion, Huazhong University of Science and Technology, Wuhan, Hubei 430074 (China); Zeng, Hancai; Zhou, Changsong; Sun, Lushi; Hu, Song; Qiu, Jianrong [State Key Laboratory of Coal Combustion, Huazhong University of Science and Technology, Wuhan, Hubei 430074 (China)

    2012-11-15

    Highlights: Black-Right-Pointing-Pointer The KI-modified BC has excellent capacity for elemental mercury removal. Black-Right-Pointing-Pointer The chemisorption plays a dominant role for the modified BC materials. Black-Right-Pointing-Pointer The BC-I has strong anti-poisoning ability with the presence of NO or SO{sub 2}. - Abstract: To develop cost-effective sorbent for gas-phase elemental mercury removal, the bamboo charcoal (BC) produced from renewable bamboo and KI modified BC (BC-I) were used for elemental mercury removal. The effect of NO, SO{sub 2} on gas-phase Hg{sup 0} adsorption by KI modified BC was evaluated on a fixed bed reactor using an online mercury analyzer. BET surface area analysis, temperature programmed desorption (TPD) and X-ray photoelectron spectroscopy (XPS) were used to determine the pore structure and surface chemistry of the sorbents. The results show that KI impregnation reduced the sorbents' BET surface area and total pore volume compared with that of the original BC. But the BC-I has excellent adsorption capacity for elemental mercury at a relatively higher temperature of 140 Degree-Sign C and 180 Degree-Sign C. The presence of NO or SO{sub 2} could inhibit Hg{sup 0} capture, but BC-I has strong anti-poisoning ability. The specific reaction mechanism has been further analyzed.

  1. Removal of mercury(II) and methylmercury from solution by tannin adsorbents

    International Nuclear Information System (INIS)

    Adsorption of mercury(II) and methylmercury by two tannin sorbents was investigated using radiotracers. High sorption capacities for mercury are registered for both sorbents at pH 7. For Eucaliptus Saligna Sm sorbent (ETS) the maximum sorption capacity was 1.2±0.2 mmol/g and for Lysiloma latisiliqua sorbent (LTS) was 8.5±0.2 mmol/g. Methylmercury adsorption maximum was recorded at pH 4 and in buffered solutions at pH 2. This species can be recovered in the presence of mercury(II). Influence of different ions present in water was examined. High recoveries were reported for ETS in tap water samples but a decrease of uptake is observed for seawater. (author)

  2. Removal performance of elemental mercury by low-cost adsorbents prepared through facile methods of carbonisation and activation of coconut husk.

    Science.gov (United States)

    Johari, Khairiraihanna; Alias, Afidatul Shazwani; Saman, Norasikin; Song, Shiow Tien; Mat, Hanapi

    2015-01-01

    The preparation of chars and activated carbon as low-cost elemental mercury adsorbents was carried out through the carbonisation of coconut husk (pith and fibre) and the activation of chars with potassium hydroxide (KOH), respectively. The synthesised adsorbents were characterised by using scanning electron microscopy, Fourier transform infrared spectroscopy and nitrogen adsorption/desorption analysis. The elemental mercury removal performance was measured using a conventional flow type packed-bed adsorber. The physical and chemical properties of the adsorbents changed as a result of the carbonisation and activation process, hence affecting on the extent of elemental mercury adsorption. The highest elemental mercury (Hg°) adsorption capacity was obtained for the CP-CHAR (3142.57 µg g(-1)), which significantly outperformed the pristine and activated carbon adsorbents, as well as higher than some adsorbents reported in the literature. PMID:25492720

  3. A one-step thermal decomposition method to prepare anatase TiO2 nanosheets with improved adsorption capacities and enhanced photocatalytic activities

    Science.gov (United States)

    Li, Wenting; Shang, Chunli; Li, Xue

    2015-12-01

    Anatase TiO2 nanosheets (NSs) with high surface area have been prepared via a one-step thermal decomposition of titanium tetraisopropoxide (TTIP) in oleylamine (OM), and their adsorption capacities and photocatalytic activities are investigated by using methylene blue (MB) and methyl orange (MO) as model pollutants. During the synthesis procedure, only one type of surfactant, oleylamine (OM), is used as capping agents and no other solvents are added. Structure and properties of the TiO2 NSs were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), N2 adsorption analysis, UV-vis spectrum, X-ray photoelectron spectroscopy (XPS) and Photoluminescence (PL) methods. The results indicate that the TiO2 NSs possess high surface area up to 378 m2 g-1. The concentration of capping agents is found to be a key factor controlling the morphology and crystalline structure of the product. Adsorption and photodegradation experiments reveal that the prepared TiO2 NSs possess high adsorption capacities of model pollutants MB and high photocatalytic activity, showing that TiO2 NSs can be used as efficient pollutant adsorbents and photocatalytic degradation catalysts of MB in wastewater treatment.

  4. Improvement of pesticide adsorption capacity of cellulose fibre by high-energy irradiation-initiated grafting of glycidyl methacrylate

    Science.gov (United States)

    Takács, Erzsébet; Wojnárovits, László; Koczog Horváth, Éva; Fekete, Tamás; Borsa, Judit

    2012-09-01

    Cellulose as a renewable raw material was used for preparation of adsorbent of organic impurities in wastewater treatment. Hydrophobic surface of cellulose substrate was developed by grafting glycidyl methacrylate in simultaneous grafting using gamma irradiation initiation. Water uptake of cellulose significantly decreased while adsorption of phenol and a pesticide molecule (2,4-dichlorophenoxyacetic acid: 2,4-D) increased upon grafting. Adsorption equilibrium data fitted the Freundlich isotherm for both solutes.

  5. Carbon nanotubes for energy storage using their hydrogen adsorption capacity: state of the art and perspectives; Nanotubos de carbono para estocagem de energia por adsorcao de hidrogenio: estado da arte e perspectivas

    Energy Technology Data Exchange (ETDEWEB)

    Maestro, Luis Fernando; Luengo, Carlos Alberto [Universidade Estadual de Campinas (UNICAMP), SP (Brazil). Inst. de Fisica. Grupo de Combustiveis Alternativos], e-mail: lmaestro@ifi.unicamp.br

    2004-07-01

    It is presented an updated scope of the research in carbon nanotubes synthesis, their purification and a discussion of recent results in energy storage using their hydrogen adsorption capacity. The GCA activities in this area are also discussed. (author)

  6. Investigations on the adsorbents for uremic middle molecular toxins (II) —Influences of crosslinking agent chain length on the adsorption capacities of crosslinked chitosan adsorbents

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Chitosan resins, which clinically served as adsorbents in hemoperfusion therapy, were prepared with reversed-phase suspension methodology using three differently structured crosslinking agents, methanal, glyoxal and glutaraldehyde. And the glyoxal and glutaraldehyde crosslinked chitosan resins were reduced with NaBH4 afterwards. By analyzing the results from FTIR and SEM, it was found that the reduction treatment to the adsorbents efficiently improved the chemical stability of these chitosan resins, and the shifts in crosslinking agents exerted influences over the morphologies of the adsorbents obviously. After being put to use in the adsorption tests upon some model uremic middle molecular toxins and BSA in vitro, all three adsorbents demon- strated a fairly realistic adsorption capability to the model toxins but little to BSA. And the adsorp- tion process reached the equilibrium in a clinically qualified short time. But the adsorption capaci- ties of these adsorbents to the model toxins were quite different. It had been found that with the growing of fatty chain length of crosslinking agent, these adsorbents showed a gradually increased adsorption capacity to the model toxins, and the glutaraldehyde crosslinked chitosan resin be- haved best.

  7. Synthesis of PGMA Microspheres with Amino Groups for High-capacity Adsorption of Cr(VI) by Cerium Initiated Graft Polymerizatio

    Institute of Scientific and Technical Information of China (English)

    李鹏飞; 杨良嵘; 何秀琼; 王娟; 孔鹏; 邢慧芳; 刘会洲

    2012-01-01

    Abstract A novel polyglycidylmethacrylate (PGMA) microspheres with high adsorption capacity of Cr(VI) was prepared by cerium(IV) initiated graft polymerization of tentacle-type polymer chains with amino group on polymer microspheres with hydroxyl groups. The micron-sized PGMA microspheres were prepared by a dispersion polym erization method and subsequently modified by ring-opening reaction to introduce functional hydroxyl groups. The polymer microspheres were characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). The results indicated that the polymer microspheres had an average diameter of 5 m with uniform size distribution. The free amino group content was determined to be 5.13 mmol·g^-1 for g;PGMA-NH2 microspheres by potentiometric and conductometric titration methods. The Cr(VI) adsorption results indicated that the graft polymerization of tentacle-type polymer chains on the polymer microspheres could produce adsorbents with high adsorption capacity (500 mg-g-l). The polymer microspheres with grafted tentacle polymer chains have potenial application in large-scale removal of Cr(VI) in aqueous solution.

  8. Surfactant-free synthesis of octahedral ZnO/ZnFe2O4 heterostructure with ultrahigh and selective adsorption capacity of malachite green

    Science.gov (United States)

    Liu, Jue; Zeng, Min; Yu, Ronghai

    2016-05-01

    A new octahedral ZnO/ZnFe2O4 heterostructure has been fabricated through a facile surfactant-free solvothermal method followed by thermal treatment. It exhibits a record-high adsorption capacity (up to 4983.0 mg·g‑1) of malachite green (MG), which is a potentially harmful dye in prevalence and should be removed from wastewater and other aqueous solutions before discharging into the environment. The octahedral ZnO/ZnFe2O4 heterostructure also demonstrates strong selective adsorption towards MG from two kinds of mixed solutions: MG/methyl orange (MO) and MG/rhodamine B (RhB) mixtures, indicating its promise in water treatment.

  9. Ultrasond-assisted synthesis of Fe3O4/SiO2 core/shell with enhanced adsorption capacity for diazinon removal

    Science.gov (United States)

    Farmany, Abbas; Mortazavi, Seyede Shima; Mahdavi, Hossein

    2016-10-01

    Fe3O4/SiO2 core/shell nanocrystals were synthesized by ultrasond-assisted procedure. The core/shell nanocrystals were characterized using XRD, FT-IR spectroscopy, SEM and BET. The BET analysis confirmed that iron oxide nanocrystal with the surface area of 208.0 m2/g can be used as an excellent adsorbent for organic and inorganic pollutants. The core/shell nanocrystal was used as an adsorbent for removal of insecticide O,O-diethyl-O[2-isopropyl-6-methylpyridimidinyl] phosphorothioate (diazinon). In continue the influence of different parameters such as pH, adsorbent dosage and shaking time on the adsorption capacity were studied. The experimental data were fitted well with the pseudo-second-order kinetic model (R2=0.9706). The adsorption isotherm was described well by Langmuir isotherm.

  10. Methane and carbon dioxide adsorption capacity of bituminous coals from the Ostrava-Karvina Coal District, Upper Silesian Basin, Czech Republic

    Science.gov (United States)

    Weniger, P.; Busch, A.; Krooss, B. M.; Francu, J.; Francu, E.

    2009-04-01

    In the context of a joint Czech-German project, experimental and analytical methods are being applied to improve the understanding of compositional variation of coal-related gas in the SW part of the Upper Silesian Basin (Czech Republic). According to present understanding, the gas composition is controlled by generation (thermal vs. microbial), migration and adsorption/desorption processes. In particular the effects of the sorption processes on the chemical and isotopic composition of coal gases are only poorly explored. During the first stage of this project, the gas adsorption capacity has been determined for coal samples representing the paralic Ostrava Formation (Namurian A) and the limnic Karviná Formation (Namurian B-C). For this purpose, high pressure adsorption isotherms have been measured for methane and carbon dioxide on medium and low volatile bituminous coal (VRr 1.2-1.8%) from the production face of two collieries in the study area. Adsorption isotherms have been measured for pressures up to 25 MPa for CO2 and up to 17 MPa for methane at 20˚ C and 45˚ C. Isotherms were measured on dry, moisture-equilibrated and "as received" samples (moisture content: 0.5-1.7%, mineral-matter-free) using a manometric method. Sorption capacities for CH4 at 45˚ C ranged from 18 to 27 Std. cm3/g (0.7 to 1.1 mmol/g) coal, dry ash-free (daf), showing an increase of sorption capacity with increasing coal rank. For CO2, sorption capacities were generally higher than for methane, ranging from 35-40 Std. cm3/g (1.4-1.7 mmol/g) coal (daf). Equilibrium moisture contents, determined by a modified ASTM method, were significantly higher than the "as received" moisture. Sorption capacities measured on moisture-equilibrated samples were generally lower than those measured on dry or "as received" samples. Methane excess sorption isotherms show a type I Langmuir form and could be approximated using the Langmuir function. Excess sorption isotherms for CO2 show a decrease in

  11. Removal of mercury from an alumina refinery aqueous stream.

    Science.gov (United States)

    Mullett, Mark; Tardio, James; Bhargava, Suresh; Dobbs, Charles

    2007-06-01

    Digestion condensate is formed as a by-product of the alumina refinery digestion process. The solution exhibits a high pH and is chemically reducing, containing many volatile species such as water, volatile organics, ammonia, and mercury. Because digestion condensate is chemically unique, an innovative approach was required to investigate mercury removal. The mercury capacity and adsorption kinetics were investigated using a number of materials including gold, silver and sulphur impregnated silica and a silver impregnated carbon. The results were compared to commercial sorbents, including extruded and powdered virgin activated carbons and a sulphur impregnated mineral. Nano-gold supported on silica (88% removal under batch conditions and 95% removal under flow conditions) and powdered activated carbon (91% under batch conditions and 98% removal under flow conditions) were the most effective materials investigated. The silver and sulphur impregnated materials were unstable in digestion condensate under the test conditions used.

  12. Adsorption of Hg(II) from aqueous solutions using TiO2 and titanate nanotube adsorbents

    Science.gov (United States)

    López-Muñoz, María-José; Arencibia, Amaya; Cerro, Luis; Pascual, Raquel; Melgar, Álvaro

    2016-03-01

    Titania and titanate nanotubes were evaluated as adsorbents for the removal of Hg(II) from aqueous solution. Commercial titanium dioxide (TiO2-P25, Evonik), a synthesized anatase sample obtained by the sol-gel method (TiO2-SG) and titanate nanotubes (TNT) prepared via hydrothermal treatment were compared. Mercury adsorption was analysed by kinetic and equilibrium experiments, studying the influence of pH and the type of adsorbents. The kinetics of Hg(II) adsorption on titania and titanate nanotubes could be well described by the pseudo-second order model. It was found that the process is generally fast with small differences between adsorbents, which cannot be explained by their dissimilarities in textural properties. Equilibrium isotherm data were best fitted with the Sips isotherm model. The maximum adsorption capacities of Hg(II) were achieved with titanate nanotubes sample, whereas between both titania samples, TiO2-SG exhibited the highest mercury uptake. For all adsorbents, adsorption capacities were enhanced as pH was increased, achieving at pH 10 Hg(II) adsorption capacities of 100, 121, and 140 mg g-1 for TiO2-P25, TiO2-SG, and TNT, respectively. Differences between samples were discussed in terms of their crystalline phase composition and chemical nature of both, mercury species and surface active sites.

  13. Adsorption of reovirus to clay minerals: effects of cation-exchange capacity, cation saturation, and surface area.

    OpenAIRE

    Lipson, S M; Stotzky, G

    1983-01-01

    The adsorption of reovirus to clay minerals has been reported by several investigators, but the mechanisms defining this association have been studied only minimally. The purpose of this investigation was to elucidate the mechanisms involved with this interaction. More reovirus type 3 was adsorbed, in both distilled and synthetic estuarine water, by low concentrations of montmorillonite than by comparable concentrations of kaolinite containing a mixed complement of cations on the exchange com...

  14. Stabilization/solidification (S/S) of mercury-contaminated hazardous wastes using thiol-functionalized zeolite and Portland cement.

    Science.gov (United States)

    Zhang, Xin-Yan; Wang, Qi-Chao; Zhang, Shao-Qing; Sun, Xiao-Jing; Zhang, Zhong-Sheng

    2009-09-15

    Stabilization/solidification (S/S) of mercury-containing solid wastes using thiol-functionalized zeolite and cement was investigated in this study. The thiol-functionalized zeolite (TFZ) used in the study was obtained by grafting the thiol group (-SH) to the natural clinoptilolite zeolites, and the mercury adsorption by TFZ was investigated. TFZ was used to stabilize mercury in solid wastes, and then the stabilized wastes were subjected to cement solidification to test the effectiveness of the whole S/S process. The results show that TFZ has a high level of -SH content (0.562 mmol g(-1)) and the adsorption of mercury by TFZ conform to the Freundlich adsorption isotherm. The mercury adsorption capacity is greatly enhanced upon thiol grafting, the maximum of which is increased from 0.041 mmol Hg g(-1) to 0.445 mmol Hg g(-1). TFZ is found to be effective in stabilizing Hg in the waste surrogate. In the stabilization process, the optimum pH for the stabilization reaction is about 5.0. The optimum TFZ dosage is about 5% and the optimum cement dosage is about 100%. Though Cl(-) and PO(4)(3-) have negative effects on mercury adsorption by TFZ, the Portland cement solidification of TFZ stabilized surrogates containing 1000 mg Hg/kg can successfully pass the TCLP leaching test. It can be concluded that the stabilization/solidification process using TFZ and Portland cement is an effective technology to treat and dispose mercury-containing wastes. PMID:19376646

  15. Dye-adsorption capacity of bituminous fly ash and its pozzolanic property after used as dye-adsorbent

    Directory of Open Access Journals (Sweden)

    Penpolcharoen, M.

    2004-02-01

    Full Text Available Bituminous fly ash, which is an industrial waste, was used as an adsorbent to remove dyestuff from the textile-dye wastewater. The batch kinetic and isotherm experiments of the synthetic wastewater were firstly conducted to determine the adsorption behavior and optimal conditions for adsorption. The optimal conditions were then applied to the actual textile-dye wastewater. Under the original conditions of fly ash and wastewater, the results indicated that the color could be removed up to 86.65% by 12 g of the fly ash /L of the wastewater within 30 min. Its adsorption was described by the Freundlich isotherm. The dye-adsorbed fly ash was further studied on its pozzolanic property in terms of compressive strength by using it as a partial substitute to Portland cement type I to produce mortar. The result revealed that the highest compressive strength was of the sample containing 10% by weight of the dye-adsorbed fly ash in replacement of cement. It possessed 215 kg/cm2 at 28 days, which is 92.67% of the sample containing 10% by weight of the original fly ash in replacement of cement, or 83.33 of the cement mortar. For the environmental concern, leachabilities of lead (Pb, chromium (Cr, copper (Cu and zinc (Zn from all mortars were also carried out. No leaching of the heavy metals from any samples could be detected. Hence, the dye-adsorbed fly ash can be used as an environmental friendly construction material.

  16. Enhancement in CO2 Adsorption Capacity and Selectivity in the Chalcogenide Aerogel CuSb2S4 by Post-synthetic Modification with LiCl

    KAUST Repository

    Ahmed, Ejaz

    2015-09-11

    The new chalcogel CuSb2S4 was obtained by reacting Cu(OAc)2·H2O with KSbS2 in a water/formamide mixture at room temperature. In order to modify the gas adsorption capacity the synthesized CuSb2S4 aerogel was loaded with different amounts of LiCl. CO2 adsorption measurements on the CuSb2S4 aerogel before and after treatment with LiCl showed more than three times increased uptake of the LiCl-modified chalcogel. The selectivities of the gas pairs CO2/H2 and CO2/CH4 in the LiCl-treated chalcogel are 235 and 105 respectively and amongst the highest reported for chalcogenide-based aerogels. In comparison with other porous materials like zeolites, activated carbon and most of the Metal Organic Frameworks (MOFs) or Porous Organic Frameworks (POFs), our synthesized aerogels show good air and moisture stability. Although, the CO2 storage capacity of our aerogels is relatively low, however the selectivity of CO2 over H2 or CH4 in LiCl-loaded aerogels are higher than in zeolites, activated carbon as well as some MOFs like Cu-BTC and MOF-5 etc.

  17. Effect of cetyl trimethyl ammonium bromide concentration on structure, morphology and carbon dioxide adsorption capacity of calcium hydroxide based sorbents

    Science.gov (United States)

    Hlaing, Nwe Ni; Vignesh, K.; Sreekantan, Srimala; Pung, Swee-Yong; Hinode, Hirofumi; Kurniawan, Winarto; Othman, Radzali; Thant, Aye Aye; Mohamed, Abdul Rahman; Salim, Chris

    2016-02-01

    Calcium hydroxide (Ca(OH)2) has been proposed as an important material for industrial, architectural, and environmental applications. In this study, calcium acetate was used as a precursor and cetyl trimethyl ammonium bromide (CTAB) was used as a surfactant to synthesize Ca(OH)2 based adsorbents for carbon dioxide (CO2) capture. The effect of CTAB concentration (0.2-0.8 M) on the structure, morphology and CO2 adsorption performance of Ca(OH)2 was studied in detail. The synthesized samples were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, field emission scanning electron microscopy (FESEM), BET surfaced area and thermogravimetry-differential thermal analysis (TG-DTA) techniques. The phase purity, crystallite size, Brunauer-Emmett-Teller (BET) surface area and CO2 adsorption performance of Ca(OH)2 precursor adsorbents were significantly increased when the concentration of CTAB was increased. XRD results showed that pure Ca(OH)2 phase was obtained at the CTAB concentration of 0.8 M. TGA results exhibited that 0.8 M of CTAB-assisted Ca(OH)2 precursor adsorbent possessed a residual carbonation conversion of ∼56% after 10 cycles.

  18. Polyamine-Cladded 18-Ring-Channel Gallium Phosphites with High-Capacity Hydrogen Adsorption and Carbon Dioxide Capture.

    Science.gov (United States)

    Sie, Ming-Jhe; Lin, Chia-Her; Wang, Sue-Lein

    2016-06-01

    In this study, we synthesized a unique inorganic framework bearing the largest 18-membered-ring channels in gallium phosphites, denoted as NTHU-15, which displayed genuine porosity even though large organic templates were present. The idea of using the "template-cladded" strategy succeeded in releasing channel space of up to ∼24% of the unit-cell volume as highly positive-charged organic templates were manipulated to cling to the anionic inorganic walls. NTHU-15 showed both high H2 uptake of 3.8 mmol/g at 77 K and effective CO2 adsorption of ∼2.4 mmol/g at 298 K, which surpassed those of all other known extra-large-channel inorganic framework structures. NTHU-15 has been successful at overcoming the long-standing problem of organic-templated extra-large-channel structures as opposed to a "true open" framework. Moreover, it realized practical gas sorption functionality in innovated metal phosphites. In view of its high stability in hot water and high selectivity for CO2 adsorption, NTHU-15 may be the first novel inorganic framework material to be applied to the field of flue gas cleaning. PMID:27181272

  19. New V(IV)-based metal-organic framework having framework flexibility and high CO2 adsorption capacity.

    Science.gov (United States)

    Liu, Ying-Ya; Couck, Sarah; Vandichel, Matthias; Grzywa, Maciej; Leus, Karen; Biswas, Shyam; Volkmer, Dirk; Gascon, Jorge; Kapteijn, Freek; Denayer, Joeri F M; Waroquier, Michel; Van Speybroeck, Veronique; Van Der Voort, Pascal

    2013-01-01

    A vanadium based metal-organic framework (MOF), VO(BPDC) (BPDC(2-) = biphenyl-4,4'-dicarboxylate), adopting an expanded MIL-47 structure type, has been synthesized via solvothermal and microwave methods. Its structural and gas/vapor sorption properties have been studied. This compound displays a distinct breathing effect toward certain adsorptives at workable temperatures. The sorption isotherms of CO(2) and CH(4) indicate a different sorption behavior at specific temperatures. In situ synchrotron X-ray powder diffraction measurements and molecular simulations have been utilized to characterize the structural transition. The experimental measurements clearly suggest the existence of both narrow pore and large pore forms. A free energy profile along the pore angle was computationally determined for the empty host framework. Apart from a regular large pore and a regular narrow pore form, an overstretched narrow pore form has also been found. Additionally, a variety of spectroscopic techniques combined with N(2) adsorption/desorption isotherms measured at 77 K demonstrate that the existence of the mixed oxidation states V(III)/V(IV) in the titled MOF structure compared to pure V(IV) increases the difficulty in triggering the flexibility of the framework. PMID:23256823

  20. Study and analysis of two semi-humid flue acid gas industrial treatment processes and study of an adsorption process of gaseous mercury on active carbon; Etude et analyse de deux dispositifs industriels de traitement d'effluents gazeux acide par voie semi-humide et etude d'un procede d'elimination du mercure gazeux par adsorption sur charbon actif

    Energy Technology Data Exchange (ETDEWEB)

    Anki, F.

    1998-07-01

    During the process of waste incineration, gaseous pollutants contained in fumes such as hydrochloric acid or mercury have to be removed before being discharged in air. A study has then been conducted on incineration plant fumes (municipal and industrial wastes). Four alkaline reagents have been tested in two semi-humid fume treatment processes for neutralizing hydrochloric acid. The reagents are: hydrated lime, sodium hydroxide, sodium bicarbonate and sodium carbonate. The alkaline solutions, pulverized in thin droplets, absorb and neutralize thus HCl and lead to the formation of a solid residue. On the other hand, a study of the adsorption of gaseous mercury on a coconut-based activated carbon has been conducted with a pilot fixed bed reactor. The taken incineration fume (flow rate: 2000 L/H) is introduced in the reactor at temperatures between 150 and 200 degrees Celsius. Different exposure times are tested to determine the saturation of the activated carbon by mercury. An evaporation model and an absorption model are applied; they represent the experimental evolution of the HCl absorption rates in terms of the liquid flow or of the stoichiometric factor. A model of mercury adsorption by the activated carbon is applied for determining the total transfer coefficient and the adsorption equilibrium constant. (O.M.)

  1. 低分子量N-羧丁酰壳聚糖的合成及其吸湿保湿性%Synthesis, Moisture Adsorption and Moisture Retention Capacities of Low Molecular Weight N-Succinyl-chitosan

    Institute of Scientific and Technical Information of China (English)

    王丽; 汪琴; 王爱勤

    2005-01-01

    Low molecular weight N-succinyl-chitosans with different degrees of substitution were synthesized by controlling reaction temperature, reaction time, and the molar ratio of the low molecular weight chitosan to succinic anhydride. The structure of the low molecular weight N-succinyl-chitosan was characterized by infrared spectroscopy(IR), by which —COCH2CH2 COOH was proved to be introduced to the —NH2 of the low molecular weight chitosan. The moisture adsorption and moisture retention capacities of the low molecular weight chitosan derivatives with different degrees of substitution were investigated. The results indicate that the moisture adsorption and moisture retention capacities of the low molecular weight N-succinyl-chitosan increase with the increase of the degree of substitution. When the degree of substitution is greater than 38%, the derivatives have better moisture adsorption and moisture retention capacities than hyaluronic acid.

  2. Study on Coal and Rock Maceral Composition Affected to Methane Adsorption Capacity%煤岩显微组成对甲烷吸附能力的影响研究

    Institute of Scientific and Technical Information of China (English)

    李振涛; 姚艳斌; 周鸿璞; 白小虎

    2012-01-01

    In order to analyze the coal maceral composition affected to the methane adsorption, the systematic tests were conducted on coal quality, coal and rock maceral composition and methane isothermal adsorption relationship of 49 coal samples from 11 coalfields in Qaidam Basin, Ordos Basin, Qinshui Basin, and other basins. The results showed that the methane adsorption capacity of the low and medium ranking coal would be increased with the vitrinite content increased and the adsorption capacity of the high ranking coal would be decreased with the vitrinite content increased. The inertinite content would have a high influence to the coal methane adsorption capacity. The methane adsorption capacity of high ranking coal would be increased with the inertinite content increased and the methane adsorption capacity of the low and medium ranking coal would be firstly increased with the inertinite content increased and then decreased in tenden- cy. When the fusinite content in low and medium ranking coal was lower, the semifusinite content in the low and medium ranking coal would be higher and the coal adsorption capacity would be stronger. The coal adsorption capacity of low ranking coal and the exinite would be in a negative correlation.%为分析煤岩显微组分对甲烷吸附作用的影响,对我国柴达木、鄂尔多斯和沁水等盆地的11个煤田49个煤样的煤质、煤岩显微组分和甲烷等温吸附关系进行了系统试验。结果表明:低、中煤阶煤的甲烷吸附能力随镜质组含量的增加而增加,而高煤阶煤的吸附能力则随之增加而降低。惰质组含量对煤吸附甲烷能力的影响较大,高煤阶煤的甲烷吸附能力随惰质组含量的增加而增加,而低、中煤阶煤的甲烷吸附能力则随之增加呈先增加后降低的趋势。低、中煤阶煤中的丝质体含量越低、半丝质体含量越高,煤的吸附能力越强。低煤阶煤吸附甲烷的能力与壳质组呈负相关关系。

  3. Characterization of Fly Ash from Coal-Fired Power Plant and Their Properties of Mercury Retention

    Science.gov (United States)

    He, Ping; Jiang, Xiumin; Wu, Jiang; Pan, Weiguo; Ren, Jianxing

    2015-12-01

    Recent research has shown that fly ash may catalyze the oxidation of elemental mercury and facilitate its removal. However, the nature of mercury-fly ash interaction is still unknown, and the mechanism of mercury retention in fly ash needs to be investigated more thoroughly. In this work, a fly ash from a coal-fired power plant is used to characterize the inorganic and organic constituents and then evaluate its mercury retention capacities. The as-received fly ash sample is mechanically sieved to obtain five size fractions. Their characteristics are examined by loss on ignition (LOI), scanning electron microscope (SEM), energy dispersive X-ray detector (EDX), X-ray diffraction (XRD), and Raman spectra. The results show that the unburned carbon (UBC) content and UBC structural ordering decrease with a decreasing particle size for the five ashes. The morphologies of different size fractions of as-received fly ash change from the glass microspheres to irregular shapes as the particle size increases, but there is no correlation between particle size and mineralogical compositions in each size fraction. The adsorption experimental studies show that the mercury-retention capacity of fly ash depends on the particle size, UBC, and the type of inorganic constituents. Mercury retention of the types of sp2 carbon is similar to that of sp3 carbon.

  4. Modification of ASM3 for the determination of biomass adsorption/storage capacity in bulking sludge control.

    Science.gov (United States)

    Makinia, J; Rosenwinkel, K H; Phan, L C

    2006-01-01

    The selector activated sludge (SAS) systems are known to prevent excessive growth of filamentous microorganisms responsible for bulking sludge, but these systems were hardly ever modelled. This study aimed to develop a model capable of predicting rapid substrate removal in the SAS systems. For this purpose, the Activated Sludge Model No. 3 (ASM3) was extended with three processes (adsorption, direct growth on the adsorbed substrate under aerobic or anoxic conditions). The modified ASM3 was tested against the results of batch experiments with the biomass originating from two full-scale SAS systems in Germany. The endogenous biomass was mixed with various readily biodegradable substrates (acetate, peptone, glucose and wastewater) and the utilisation of substrate (expresses as COD) and oxygen uptake rates (OURs) were measured during the experiments. In general, model predictions fitted to the experimental data, but a considerable number of kinetic (5) and stoichiometric (2) parameters needed to be adjusted during model calibration. The simulation results revealed that storage was generally a dominating process compared to direct growth in terms of the adsorbed substrate utilisation. The contribution of storage ranged from 65-71% (Plant A) and 69-92% (Plant B). PMID:16605021

  5. Synthesis of fungus-like MoS2 nanosheets with ultrafast adsorption capacities toward organic dyes

    Science.gov (United States)

    Song, HaoJie; You, Shengsheng; Jia, XiaoHua

    2015-11-01

    Fungus-like molybdenum disulfide (MoS2) nanosheets with a thickness of a few nanometers have been successfully synthesized via one-pot hydrothermal method. The as-prepared MoS2 nanosheets with a high surface area of 106.989 m2 g-1 exhibited excellent wastewater treatment performance with high removal capacities toward organic dyes. In addition, the fungus-like MoS2 nanosheets can absorb Congo red completely within 2 min. Successful access to high quality fungus-like MoS2 nanosheets will make it possible for their potential application in catalysis and other fields.

  6. A new specific polymeric material for mercury speciation: Application to environmental and food samples.

    Science.gov (United States)

    Zarco-Fernández, S; Mancheño, M J; Muñoz-Olivas, R; Cámara, C

    2015-10-15

    A new polymeric material (Patent: P201400535) highly specific for mercury is presented. Its great capability to pre-concentrate and selectively elute inorganic mercury and methylmercury are the main figures of merit. The polymer can be reused several times. To our knowledge, this is the only polymer proposed in the literature for direct inorganic mercury and methylmercury speciation without need of chromatography or quantification by difference. The polymer formation is based on the reaction of a vinyl derivative of 8-hydroxiquinoline as monomer, and 2-(Methacryloylamino) ethyl 2-Methyl Acrylate (NOBE) as co-monomer. Random radical polymerization by the precipitation method was carried out using Azobisisobutyronitrile (AIBN) as initiator. The polymer was characterized by SEM and FTIR. Adsorption binding isotherms were evaluated using Langmuir and Freundlich models, showing high adsorption capacity for both inorganic and organic mercury species. The polymer was employed to sequentially determine inorganic mercury and methylmercury, using a solid phase extraction (SPE) scheme. Cross reactivity of several ions, as well as matrix effects from a high saline matrix like seawater was irrelevant as the retained fractions mostly eluted during the washing step. The procedure was first validated by analyzing a certified reference material (BCR 464) and finally applied to commercial fish samples. The speciation proposed procedure is cheap, fast, and easy to use and minimizes reagents waste.

  7. Mercury release from deforested soils triggered by base cation enrichment.

    Science.gov (United States)

    Farella, N; Lucotte, M; Davidson, R; Daigle, S

    2006-09-01

    The Brazilian Amazon has experienced considerable colonization in the last few decades. Family agriculture based on slash-and-burn enables millions of people to live in that region. However, the poor nutrient content of most Amazonian soils requires cation-rich ashes from the burning of the vegetation biomass for cultivation to be successful, which leads to forest ecosystem degradation, soil erosion and mercury contamination. While recent studies have suggested that mercury present in soils was transferred towards rivers upon deforestation, little is known about the dynamics between agricultural land-use and mercury leaching. In this context, the present study proposes an explanation that illustrates how agricultural land-use triggers mercury loss from soils. This explanation lies in the competition between base cations and mercury in soils which are characterized by a low adsorption capacity. Since these soils are naturally very poor in base cations, the burning of the forest biomass suddenly brings high quantities of base cations to soils, destabilizing the previous equilibrium amongst cations. Base cation enrichment triggers mobility in soil cations, rapidly dislocating mercury atoms. This conclusion comes from principal component analyses illustrating that agricultural land-use was associated with base cation enrichment and mercury depletion. The overall conclusions highlight a pernicious cycle: while soil nutrient enrichment actually occurs through biomass burning, although on a temporary basis, there is a loss in Hg content, which is leached to rivers, entering the aquatic chain, and posing a potential health threat to local populations. Data presented here reflects three decades of deforestation activities, but little is known about the long-term impact of such a disequilibrium. These findings may have repercussions on our understanding of the complex dynamics of deforestation and agriculture worldwide. PMID:16781764

  8. Synthesis of fungus-like MoS{sub 2} nanosheets with ultrafast adsorption capacities toward organic dyes

    Energy Technology Data Exchange (ETDEWEB)

    Song, HaoJie; You, Shengsheng [Jiangsu University, School of Materials Science and Engineering, Zhenjiang, Jiangsu (China); Jia, XiaoHua [Jiangsu University, School of Environment and Safety Engineering, Zhenjiang, Jiangsu (China)

    2015-11-15

    Fungus-like molybdenum disulfide (MoS{sub 2}) nanosheets with a thickness of a few nanometers have been successfully synthesized via one-pot hydrothermal method. The as-prepared MoS{sub 2} nanosheets with a high surface area of 106.989 m{sup 2} g{sup -1} exhibited excellent wastewater treatment performance with high removal capacities toward organic dyes. In addition, the fungus-like MoS{sub 2} nanosheets can absorb Congo red completely within 2 min. Successful access to high quality fungus-like MoS{sub 2} nanosheets will make it possible for their potential application in catalysis and other fields. (orig.)

  9. Removal of mercury from water using pottery

    International Nuclear Information System (INIS)

    In a previous study, the sorption of radiocobalt by powdered pottery materials was investigated. The use of these materials as immobilization matrix for liquid radioactive waste requires the employment of pottery vessels. Therefore, the present study aims to give detailed investigations of the decontamination of radionuclides and toxic elements using pottery containers. These investigations are equally useful to elucidate how far these vessels can be utilized for water purification through decontamination of toxic and heavy metals. The radionuclide or heavy metal removal capability using pottery pots, as low cost sorbents, has been investigated for both radioactive (203Hg) and stable mercury. The results indicated that Hg2+ is better removed by pottery from neutral to alkaline solutions. The capacity of the used pottery container (100 ml in volume) for complete removal of mercury was found to reach 3 x 10-4 mol/l, and the time needed was 8 hours. The sorption process was suggested to occur via adsorption and ion exchange. The effect of presence of humic or fulvic acid, as ligands abundant in water, is also investigated. The results imply that, in absence of humic or fulvic acid the sorption follows the expected behaviour, i.e. sorption sites with similar affinity for mercury. In presence of humic or fulvic acid, additional sorption sites are available by the organic molecule when it is associated to the pottery. (orig.)

  10. Effect of diet on the capacity to remove mercury from the body of a penguin (Spheniscus demersus) living in the ZOO

    OpenAIRE

    Falkowska L.; Szumiło E.; Hajdryh J.; Grajewska A.; Bełdowska M.; Krause I

    2013-01-01

    Birds due to its position in the trophic chain are good monitors of the marine environment in terms of mercury contamination. For the proper interpretation of results it is necessary to know both the processes of accumulation of this metal in their bodies and processes of elimination. Research involving the Penguin (Spheniscus demersus) living in a ZOO has identified the relationship between diet and the amount of mercury removed from the penguin body in guano, feathers, and in the case of fe...

  11. Effect of diet on the capacity to remove mercury from the body of a penguin (Spheniscus demersus living in the ZOO

    Directory of Open Access Journals (Sweden)

    Falkowska L.

    2013-04-01

    Full Text Available Birds due to its position in the trophic chain are good monitors of the marine environment in terms of mercury contamination. For the proper interpretation of results it is necessary to know both the processes of accumulation of this metal in their bodies and processes of elimination. Research involving the Penguin (Spheniscus demersus living in a ZOO has identified the relationship between diet and the amount of mercury removed from the penguin body in guano, feathers, and in the case of females with eggs. The research was conducted in years 2009-2011. Total mercury was determined in elements responsible for detoxification and in the diet of penguins. Mercury concentration was determined by atomic absorption spectrophotometry with AMA-254 automatic mercury analyzer. The highest average mercury concentrations were determined in feathers: 1781.12 ngHg•g−1d.w., lower in eggs: 950.88 ngHg•g−1 dry weight (d.w.. and in a guano: 139.18 ngHg•g−1. In food, herrings caught in the southern Baltic, Hg concentrations were relatively low with averaged value 31.81 ngHg•g−1d.w.

  12. Single-Walled Carbon Nanotubes (SWCNTs), as a Novel Sorbent for Determination of Mercury in Air

    Science.gov (United States)

    Golbabaei, Farideh; Ebrahimi, Ali; Shirkhanloo, Hamid; Koohpaei, Alireza; Faghihi-Zarandi, Ali

    2016-01-01

    Background: Based on the noticeable toxicity and numerous application of mercury in industries, removal of mercury vapor through sorbent is an important environmental challenge. Purpose of the Study: Due to their highly porous and hollow structure, large specific surface area, light mass density and strong interaction, Single-Walled Carbon Nanotubes (SWCNTs) sorbent were selected for this investigation. Methods: In this study, instrumental conditions, method procedure and different effective parameters such as adsorption efficiency, desorption capacity, time, temperature and repeatability as well as retention time of adsorbed mercury were studied and optimized. Also, mercury vapor was determined by cold vapor atomic absorption spectrometry (CV-AAS). Obtained data were analyzed by Independent T- test, Multivariate linear regression and one way–ANOVA finally. Results: For 80 mg nanotubes, working range of SWCNT were achieved 0.02-0.7 μg with linear range (R2=0.994). Our data revealed that maximum absorption capacity was 0.5 μg g-1 as well as limit of detection (LOD) for studied sorbent was 0.006 μg. Also, optimum time and temperature were reported, 10 min and 250 °C respectively. Retention time of mercury on CNTs for three weeks was over 90%. Results of repeated trials indicated that the CNTs had long life, so that after 30 cycles of experiments, efficiency was determined without performance loss. Conclusion: Results showed that carbon nanotubes have high potential for efficient extraction of mercury from air and can be used for occupational and environmental purposes. The study of adsorption properties of CNTs is recommended.

  13. Adsorption of Ag, Cu and Hg from aqueous solutions using expanded perlite

    International Nuclear Information System (INIS)

    The aim of the present work was to investigate the ability of expanded perlite (EP) to remove of silver, copper and mercury ions from aqueous solutions. Batch adsorption experiments were carried out and the effect of pH, adsorbent dosage, contact time and temperature of solution on the removal process has been investigated. The optimum pH for the adsorption was found to be 6.5. Adsorption of these metal ions reached their equilibrium concentration in 120, 240 and 180 min for Ag (I), Cu (II) and Hg (II) ions, respectively. Experimental data were also evaluated in terms of kinetic characteristics of adsorption and it was found that adsorption process for these metal ions followed well pseudo-second-order kinetics. Using Langmuir isotherm model, maximum adsorption capacity of EP was found to be 8.46, 1.95 and 0.35 mg/g for Ag (I), Cu (II) and Hg (II) ions, respectively. Finally, the thermodynamic parameters including, the change of free energy (ΔGo), enthalpy (ΔHo) and entropy (ΔSo) of adsorption were calculated for each metal ion. The results showed that the adsorption of these metal ions on EP was feasible and exothermic at 20-50 deg. C.

  14. Adsorption of Ag, Cu and Hg from aqueous solutions using expanded perlite.

    Science.gov (United States)

    Ghassabzadeh, Hamid; Mohadespour, Ahmad; Torab-Mostaedi, Meisam; Zaheri, Parisa; Maragheh, Mohammad Ghannadi; Taheri, Hossein

    2010-05-15

    The aim of the present work was to investigate the ability of expanded perlite (EP) to remove of silver, copper and mercury ions from aqueous solutions. Batch adsorption experiments were carried out and the effect of pH, adsorbent dosage, contact time and temperature of solution on the removal process has been investigated. The optimum pH for the adsorption was found to be 6.5. Adsorption of these metal ions reached their equilibrium concentration in 120, 240 and 180 min for Ag (I), Cu (II) and Hg (II) ions, respectively. Experimental data were also evaluated in terms of kinetic characteristics of adsorption and it was found that adsorption process for these metal ions followed well pseudo-second-order kinetics. Using Langmuir isotherm model, maximum adsorption capacity of EP was found to be 8.46, 1.95 and 0.35 mg/g for Ag (I), Cu (II) and Hg (II) ions, respectively. Finally, the thermodynamic parameters including, the change of free energy (DeltaG degrees ), enthalpy (DeltaH degrees ) and entropy (DeltaS degrees ) of adsorption were calculated for each metal ion. The results showed that the adsorption of these metal ions on EP was feasible and exothermic at 20-50 degrees C.

  15. Mercury and Your Health

    Science.gov (United States)

    ... the Risk of Exposure to Mercury Learn About Mercury What is Mercury What is Metallic mercury? Toxicological Profile ToxFAQs Mercury Resources CDC’s National Biomonitoring Program Factsheet on Mercury ...

  16. 改性沸石和膨润土对氟离子吸附性能研究%Study on the adsorption capacity of modified zeoIite and bentonite for fIuoride ions

    Institute of Scientific and Technical Information of China (English)

    赵文生; 孙彦红; 赵万明

    2016-01-01

    High-temperature roasting,sulphuric acid,and magnesium sulphate have been used for the modification of natural zeolite and bentonite. The effects of three kinds of modification methods on the adsorption capacity of zeo-lite and bentonite for fluoride ions have been investigated. The experimental results show that high-temperature roasting,sulphuric acid modification and magnesium sulphate modification can all increase the adsorption capacity of zeolite and bentonite for fluoride ions. The adsorption of modified zeolite for fluoride ions complies with Langmuir isothermal adsorption;the adsorption of sulphuric acid modified and magnesium sulphate modified bentonite for fluo-ride ions can be described with both Langmuir model and Freundlich model;while the adsorption of high-tempera-ture roasting modified bentonite for fluoride ions complies with Freundlich model.%选用高温焙烧、硫酸、硫酸镁改性天然沸石和膨润土,考察了3种改性方法对沸石和膨润土吸附氟离子性能的影响。实验结果表明,高温焙烧、硫酸改性和硫酸镁改性均提高了沸石和膨润土对氟离子的吸附能力。改性沸石对氟离子的吸附符合Langmuir等温吸附模型;硫酸改性、硫酸镁改性膨润土对氟离子的吸附可用Langmuir模型和Freundlich模型描述,高温焙烧改性膨润土对氟离子的吸附则符合Freundlich模型。

  17. Chelating capacity and the adverse effects of two treatments (N-acetylcysteine and D-penicillamine in patients with mercury poisoning in Segovia, a municipality at the northeastern part of Antioquia, Colombia

    Directory of Open Access Journals (Sweden)

    Fanny Cuesta González

    2008-02-01

    Full Text Available

    OBJECTIVE: to compare the chelating capacity and the adverse effects of treatments with either Nacetylcysteine or D-penicillamine in patients with mercury poisoning in Segovia, a municipality at the northeastern part of Antioquia, Colombia.

    METHODS: 50 patients with toxic levels of mercury were enrolled in a 10 days open label, randomized comparison of either D-penicillamine (750 mg/day or Nacetilcysteine (1.8 g/day. Patients were followed on a daily basis to assess the elimination of mercury in urine and the frequency of adverse effects of each treatment.

    RESULTS: 32 patients completed 10 days of drug treatment. Averages of mercury elimination in 24 hours urine, before and after treatment with D-penicillamine and N-acetylcysteine, were not different (211.96 mcg ± 190 and 262.15 mcg ± 305 and 232.85 mcg ± 248 and 218.65 mcg ± 240, respectively, P > 0.05 for all comparisons. Evaluation of the frequency of adverse effects showed a significant difference between the two groups: D-penicillamine (50% and N-acetylcysteine (11% p = 0.0079.

    CONCLUSION: this study

  18. Different crystal-forms of one-dimensional MnO2 nanomaterials for the catalytic oxidation and adsorption of elemental mercury.

    Science.gov (United States)

    Xu, Haomiao; Qu, Zan; Zhao, Songjian; Mei, Jian; Quan, Fuquan; Yan, Naiqiang

    2015-12-15

    MnO2 has been found to be a promising material to capture elemental mercury (Hg(0)) from waste gases. To investigate the structure effect on Hg(0) uptake, three types of one-dimensional (1D) MnO2 nano-particles, α-, β- and γ-MnO2, were successfully prepared and tested. The structures of α-, β- and γ-MnO2 were characterized by XRD, BET, TEM and SEM. The results indicate that α-, β- and γ-MnO2 were present in the morphologies of belt-, rod- and spindle-like 1D materials, respectively. These findings demonstrated noticeably different activities in capturing Hg(0), depending on the surface area and crystalline structure. The performance enhancement is in the order of: β-MnO2removal using MnO2 was discussed with the help of results from H2-TPR, XPS and Hg(0) removal experiments in the absence of O2. It was determined that the oxidizability of three forms of MnO2 increased as follows: β-MnO2mercury and manganese oxide sites are demonstrated to increase in the following order: β-MnO2<γ-MnO2<α-MnO2 based on the desorption tests. PMID:26093358

  19. Planet Mercury

    Science.gov (United States)

    1974-01-01

    Mariner 10's first image of Mercury acquired on March 24, 1974. During its flight, Mariner 10's trajectory brought it behind the lighted hemisphere of Mercury, where this image was taken, in order to acquire important measurements with other instruments.This picture was acquired from a distance of 3,340,000 miles (5,380,000 km) from the surface of Mercury. The diameter of Mercury (3,031 miles; 4,878 km) is about 1/3 that of Earth.Images of Mercury were acquired in two steps, an inbound leg (images acquired before passing into Mercury's shadow) and an outbound leg (after exiting from Mercury's shadow). More than 2300 useful images of Mercury were taken, both moderate resolution (3-20 km/pixel) color and high resolution (better than 1 km/pixel) black and white coverage.

  20. Mercury(6)

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    31. Since Mariner Ten's flight, astronomers have been trying to find out more about Mercury. Telescopes, including the orbiting Hubble Space Telescope,cannot help much. They would be damaged by the bright light of the sun if they turned to look at Mercury. So, astronomers are studying Mercury from observatories on Earth. They are recording information about the planet's radiation.

  1. Carbonaceous materials for adsorptive refrigerators

    Science.gov (United States)

    Buczek, B.; Wolak, E.

    2012-06-01

    Carbon monoliths prepared from hard coal precursors were obtained. The porous structure of the monoliths was evaluated on the basis of nitrogen adsorption — desorption equilibrium data. The investigated monoliths have a well-developed microporous structure with significant specific surface area (S BET ). Equilibrium studies of methanol vapour adsorption were used to characterize the methanol adsorptive capacity that was determined using a volumetric method. The heat of wetting by methanol was determined in order to estimate the energetic effects of the adsorption process. The results of the investigations show that all monoliths exhibit high adsorption capacity and high heat of wetting with methanol.

  2. Characterization and application of tourmaline and beryl from Brazilian pegmatite in adsorption process with divalent metals

    Institute of Scientific and Technical Information of China (English)

    Denis L.Guerra; Silze P.Oliveira; Ricardo A.R.Silva; Victor Leidens; Adriano C.Batista

    2012-01-01

    In this study,the original tourmaline and beryl mineral samples have been collected from a Brazilian pegmatite.The objective of this study was to examine the adsorption behavior of Brazilian ciclosilicate sampies,towards divalent metals (Pb2+,Mn2+,and Zn2+) in ethanol solution has been studies by a batch technique.The ciclosilicate samples were characterized by elemental analysis,Fourier transform infrared spectroscopy,helium picnometry,mercury porosity,and nitrogen adsorption-desorption.The Langmuir expression for adsorption isotherm was applied in order to determine the adsorption capacity to form a monolayer and the constant related to the adsorption intensity.In aqueous solution there was a significant adsorption increase with the temperature and pronounced synergistic effects were observed.The maximum number of moles adsorbed was determined to be 12.48 and 11.49 mmol/g for systems Pb2+/beryl and Pb2+/tourmaline,respectively.The energetic effects caused by metal cations adsorption were determined through calorimetric titrations.Thermodynamics indicated the existence of favorable conditions for such Pb2+-,Mn2+-,and Zn2+-OH interactions.

  3. COMBINED THEORETICAL AND EXPERIMENTAL INVESTIGATION OF MECHANISMS AND KINETICS OF VAPOR-PHASE MERCURY UPTAKE BY CARBONACOUES SURFACES

    Energy Technology Data Exchange (ETDEWEB)

    Radisav D. Vidic

    2002-05-01

    The first part of this study evaluated the application of a versatile optical technique to study the adsorption and desorption of model adsorbates representative of volatile polar (acetone) and non-polar (propane) organic compounds on a model carbonaceous surface under ultra high vacuum (UHV) conditions. The results showed the strong correlation between optical differential reflectance (ODR) and adsorbate coverage determined by temperature programmed desorption (TPD). ODR technique was proved to be a powerful tool to investigate surface adsorption and desorption from UHV to high pressure conditions. The effects of chemical functionality and surface morphology on the adsorption/desorption behavior of acetone, propane and mercury were investigated for two model carbonaceous surfaces, namely air-cleaved highly oriented pyrolytic graphite (HOPG) and plasma-oxidized HOPG. They can be removed by thermal treatment (> 500 K). The presence of these groups almost completely suppresses propane adsorption at 90K and removal of these groups leads to dramatic increase in adsorption capacity. The amount of acetone adsorbed is independent of surface heat treatment and depends only on total exposure. The effects of morphological heterogeneity is evident for plasma-oxidized HOPG as this substrate provides greater surface area, as well as higher energy binding sites. Mercury adsorption at 100 K on HOPG surfaces with and without chemical functionalities and topological heterogeneity created by plasma oxidation occurs through physisorption. The removal of chemical functionalities from HOPG surface enhances mercury physisorption. Plasma oxidation of HOPG provides additional surface area for mercury adsorption. Mercury adsorption by activated carbon at atmospheric pressure occurs through two distinct mechanisms, physisorption below 348 K and chemisorption above 348 K. No significant impact of oxygen functionalities was observed in the chemisorption region. The key findings of this study

  4. Insights into the adsorption capacity and breakthrough properties of a synthetic zeolite against a mixture of various sulfur species at low ppb levels.

    Science.gov (United States)

    Vellingiri, Kowsalya; Kim, Ki-Hyun; Kwon, Eilhann E; Deep, Akash; Jo, Sang-Hee; Szulejko, Jan E

    2016-01-15

    The sorptive removal properties of a synthetic A4 zeolite were evaluated against sulfur dioxide (SO2) and four reference reduced sulfur compounds (RSC: hydrogen sulfide (H2S), methanethiol (CH3SH), dimethyl sulfide (DMS, (CH3)2S), and dimethyl disulfide (DMDS, CH3SSCH3). To this end, a sorbent bed of untreated (as-received) A4 zeolite was loaded with gaseous standards at four concentration levels (10-100 part-per-billion (ppb (v/v)) at four different volumes (0.1, 0.2, 0.5, and 1 L increments) in both increasing (IO: 0.1-1.0 L) and decreasing volume order (DO: 1.0 to 0.1 L). Morphological properties were characterized by PXRD, FTIR, and BET analysis. The removal efficiency of SO2 decreased from 100% for all concentrations at 0.1 L (initial sample volume) to ∼82% (100 ppb) or ∼96% (10 ppb) at 3.6 L. In contrast, removal efficiency of RSC was near 100% at small loading volumes but then fell sharply, irrespective of concentration (10-100 ppb) (e.g., 32% (DMS) to 52% (H2S) at 100 ppb). The adsorption capacity of zeolite, if expressed in terms of solid-gas partition coefficient (e.g., similar to the Henry's law constant (mmol kg(-1) Pa(-1))), showed moderate variabilities with the standard concentration levels and S compound types such as the minimum of 2.03 for CH3SH (at 20 ppb) to the maximum of 13.9 for SO2 (at 10 ppb). It clearly demonstrated a notable distinction in the removal efficiency of A4 zeolite among the different S species in a mixture with enhanced removal efficiency of SO2 compared to the RSCs.

  5. Bone char surface modification by nano-gold coating for elemental mercury vapor removal

    Science.gov (United States)

    Assari, Mohamad javad; Rezaee, Abbas; Rangkooy, Hossinali

    2015-07-01

    The present work was done to develop a novel nanocomposite using bone char coated with nano-gold for capture of elemental mercury (Hg0) from air. The morphologies, structures, and chemical constitute of the prepared nanocomposite were evaluated by UV-VIS-NIR, dynamic light-scattering (DLS), X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infra-red (FTIR) spectroscopy, and energy dispersive X-ray spectroscopy (EDS). The capture performance of nanocomposite was evaluated in a needle trap for mercury vapor. An on-line setup based on cold vapor atomic absorption spectrometry (CVAAS) was designed for Hg0 determination. Dynamic capacity of nanocomposite for Hg0 was shown high efficient operating capacity of 586.7 μg/g. As temperature increases, the dynamic adsorption capacity of the nanocomposite was decreased, which are characteristics of physicosorption processes. It was found that the surface modification of bone char with nano-gold has various advantages such as high operating dynamic adsorption capacity and low cost preparation. It was also demonstrated that the developed nanocomposite is suitable for on-line monitoring of Hg0. It could be applied for the laboratory and field studies.

  6. Surfactant mediated synthesis of poly(acrylic acid) grafted xanthan gum and its efficient role in adsorption of soluble inorganic mercury from water.

    Science.gov (United States)

    Pal, Abhijit; Majumder, Kunal; Bandyopadhyay, Abhijit

    2016-11-01

    Noble copolymers from xanthan gum (XG) and poly(acrylic acid) (PAA) were synthesised through surfactant mediated graft copolymerization. The copolymers were applied as a biosorbent for inorganic Hg(II) at higher concentration level (300ppm). The copolymers were characterized using different analytical techniques which showed, the grafting principally occurred across the amorphous region of XG. Measurement of zeta potential and hydrodynamic size indicated, the copolymers were strong polyanion and possessed greater hydrodynamic size (almost in all cases) than XG, despite a strong molecular degradation that took place simultaneously during grafting. In the dispersed form, all grades of the copolymer displayed higher adsorption capability than XG, however, the grade with maximum grafting produced the highest efficiency (68.03%). Manipulation produced further improvement in efficiency to 72.17% with the same copolymer after 75min at a pH of 5.0. The allowable biosorbent dose, however, was 1000ppm as determined from the experimental evidences. PMID:27516248

  7. Basic Information about Mercury

    Science.gov (United States)

    ... Twitter Google+ Pinterest Contact Us Basic Information about Mercury On this page: What is mercury? Emissions of ... Consumer products that traditionally contain mercury What is Mercury? Mercury is a naturally-occurring chemical element found ...

  8. Mercury(1)

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    1.Mercury is the planet closest to the sun.It is thefastest moving planet.And it is the second smallestplanet in our solar system. 2.Mercury is very difficult to see.Its orbit isbetween us and the sun.So,we have to look toward thebright light of the sun to see it.The sunlight usuallyhides Mercury.When we can see it,it appears as a fuzzyball.

  9. Pore Structure of Shales from High Pressure Mercury Injection and Nitrogen Adsorption Method%高压压汞法和氮气吸附法分析页岩孔隙结构

    Institute of Scientific and Technical Information of China (English)

    杨峰; 宁正福; 孔德涛; 刘慧卿

    2013-01-01

    页岩储层的孔隙结构对页岩含气性评价和勘探开发具有重要意义,但目前国内对于页岩孔隙结构的研究相对较少.为此,采用高压压汞实验和低温氮气吸附实验对页岩的孔隙结构进行了研究,计算了页岩的孔隙结构参数,并结合微观孔隙结构图片分析了页岩孔隙结构对气体吸附和渗流的意义.研究表明,页岩孔隙以微孔和过渡孔为主,微孔和过渡孔提供了大部分孔体积.有机质中的微孔是页岩比表面积的主要贡献者,构成了页岩气体的主要吸附空间.页岩的孔隙类型复杂,孔隙形态多样,存在一端封闭的不透气性孔、开放性的透气性孔和墨水瓶孔等多种孔隙,且孔隙之间的连通性较差.较高的微孔和过渡孔保证了页岩储层具有很高的吸附聚气能力,但中孔和大孔发育较差,不利于气体渗流和页岩气藏的开发.%The pore structure of shales plays an important role in the evaluation of hydrocarbon content,gas exploration and development.However,there is little study on the pore structure of shales at home.Highpressure mercury injection and nitrogen adsorption experiments are employed to study the pore structure of shales and the pore structure parameters are also obtained.The effect of pore structure on gas adsorption and movement is analyzed.The results show that micropores and transitional pores are the main pore in shales,which provide the vast majority of pore volume.Micropore in the organic matter is the primary contributor to specific surface area and functions as the main adsorption space.The pore types are complicated and the pore morphology is diverse.There are airtight pores with a close end,air pores,and ink-bottle pores in shales and the pore connectivity is poor.The high content of micropore and transitional pore is beneficial for gas adsorption in shales,but the mesopore and macropore are backward,which goes against for shale gas seepage and production.

  10. Development of Nano-Sulfide Sorbent for Efficient Removal of Elemental Mercury from Coal Combustion Fuel Gas.

    Science.gov (United States)

    Li, Hailong; Zhu, Lei; Wang, Jun; Li, Liqing; Shih, Kaimin

    2016-09-01

    The surface area of zinc sulfide (ZnS) was successfully enlarged using nanostructure particles synthesized by a liquid-phase precipitation method. The ZnS with the highest surface area (named Nano-ZnS) of 196.1 m(2)·g(-1) was then used to remove gas-phase elemental mercury (Hg(0)) from simulated coal combustion fuel gas at relatively high temperatures (140 to 260 °C). The Nano-ZnS exhibited far greater Hg(0) adsorption capacity than the conventional bulk ZnS sorbent due to the abundance of surface sulfur sites, which have a high binding affinity for Hg(0). Hg(0) was first physically adsorbed on the sorbent surface and then reacted with the adjacent surface sulfur to form the most stable mercury compound, HgS, which was confirmed by X-ray photoelectron spectroscopy analysis and a temperature-programmed desorption test. At the optimal temperature of 180 °C, the equilibrium Hg(0) adsorption capacity of the Nano-ZnS (inlet Hg(0) concentration of 65.0 μg·m(-3)) was greater than 497.84 μg·g(-1). Compared with several commercial activated carbons used exclusively for gas-phase mercury removal, the Nano-ZnS was superior in both Hg(0) adsorption capacity and adsorption rate. With this excellent Hg(0) removal performance, noncarbon Nano-ZnS may prove to be an advantageous alternative to activated carbon for Hg(0) removal in power plants equipped with particulate matter control devices, while also offering a means of reusing fly ash as a valuable resource, for example as a concrete additive.

  11. Development of Nano-Sulfide Sorbent for Efficient Removal of Elemental Mercury from Coal Combustion Fuel Gas.

    Science.gov (United States)

    Li, Hailong; Zhu, Lei; Wang, Jun; Li, Liqing; Shih, Kaimin

    2016-09-01

    The surface area of zinc sulfide (ZnS) was successfully enlarged using nanostructure particles synthesized by a liquid-phase precipitation method. The ZnS with the highest surface area (named Nano-ZnS) of 196.1 m(2)·g(-1) was then used to remove gas-phase elemental mercury (Hg(0)) from simulated coal combustion fuel gas at relatively high temperatures (140 to 260 °C). The Nano-ZnS exhibited far greater Hg(0) adsorption capacity than the conventional bulk ZnS sorbent due to the abundance of surface sulfur sites, which have a high binding affinity for Hg(0). Hg(0) was first physically adsorbed on the sorbent surface and then reacted with the adjacent surface sulfur to form the most stable mercury compound, HgS, which was confirmed by X-ray photoelectron spectroscopy analysis and a temperature-programmed desorption test. At the optimal temperature of 180 °C, the equilibrium Hg(0) adsorption capacity of the Nano-ZnS (inlet Hg(0) concentration of 65.0 μg·m(-3)) was greater than 497.84 μg·g(-1). Compared with several commercial activated carbons used exclusively for gas-phase mercury removal, the Nano-ZnS was superior in both Hg(0) adsorption capacity and adsorption rate. With this excellent Hg(0) removal performance, noncarbon Nano-ZnS may prove to be an advantageous alternative to activated carbon for Hg(0) removal in power plants equipped with particulate matter control devices, while also offering a means of reusing fly ash as a valuable resource, for example as a concrete additive. PMID:27508312

  12. Efficient removal of mercury from aqueous solutions and industrial effluent.

    Science.gov (United States)

    Dos Santos, Maria B P; Leal, Katia Z; Oliveira, Fernando J S; Sella, Silvia M; Vieira, Méri D; Marques, Elisa M D; Gomes, Vanessa A C

    2015-01-01

    The objective of this study was to examine the ability of a solid waste produced during beneficiation of ornamental rocks to remove mercury (Hg) from an industrial effluent and aqueous solutions under various conditions. Batch studies have been carried out by observing the effects of pH, concentration of the adsorbate, contact time, and so on. Various sorption isotherm models such as Langmuir, Freundlich, and Tóth have been applied for the adsorbent. Film and intraparticle diffusion were both found to be rate-limiting steps. Adsorption was properly described by the Freundlich model (capacity constant of 0.3090 (mg g(-1))(mg L(-1))(-1/n) and adsorption intensity indicator of 2.2939), which indicated a favorable sorption and encouraged subsequent studies for treatment of Hg-containing industrial effluent. Industrial effluent treatment efficiency reached Hg removals greater than 90% by using ornamental rock solid waste (ORSW). Besides, desorption studies indicated that the maximum recovery of mercury was 100 ± 2% for 1 mol L(-1) HNO3 and 74 ± 8% for 0.1 mol L(-1) HNO3. The ORSW could be reused thrice without significant difference on the Hg removal rate from industrial effluent. These findings place ORSW as a promising efficient and low-cost adsorbent for the removal of Hg from aqueous solutions and industrial effluent. PMID:26301849

  13. Modeling study of natural emissions, source apportionment, and emission control of atmospheric mercury

    Science.gov (United States)

    Shetty, Suraj K.

    ) and CAMNet (Canadian Atmospheric Mercury Measurement Network). The model estimated a total deposition of 474 Mg yr-1 to the CONUS (Contiguous United States) domain, with two-thirds being dry deposited. Reactive gaseous mercury contributed the most to 60% of deposition. Emission speciation distribution is a key factor for local deposition as contribution from large point sources can be as high as 75% near (coal combustion processes has attracted great attention due to its toxicity and the emission-control regulations and has lead to advancement in state-of-the-art control technologies that alleviate the impact of mercury on ecosystem and human health. This part of the work applies a sorption model to simulate adsorption of mercury in flue gases, onto a confined-bed of activated carbon. The model's performances were studied at various flue gas flow rates, inlet mercury concentrations and adsorption bed temperatures. The process simulated a flue gas, with inlet mercury concentration of 300 ppb, entering at a velocity of 0.3 m s-1 from the bottom into a fixed bed (inside bed diameter of 1 m and 3 m bed height; bed temperature of 25 °C) of activated carbon (particle size of 0.004 m with density of 0.5 g cm-3 and surface area of 90.25 cm2 g -1). The model result demonstrated that a batch of activated carbon bed was capable of controlling mercury emission for approximately 275 days after which further mercury uptake starts to decrease till it reaches about 500 days when additional control ceases. An increase in bed temperature significantly reduces mercury sorption capacity of the activated carbon. Increase in flue gas flow rate may result in faster consumption of sorption capacity initially but at a later stage, the sorption rate decreases due to reduced sorption capacity. Thus, overall sorption rate remains unaffected. The activated carbon's effective life (time to reach saturation) is not affected by inlet mercury concentration, implying that the designing and operation

  14. Kinetic and thermodynamic studies of Hg(II) adsorption onto MCM-41 modified by ZnCl2

    Science.gov (United States)

    Raji, Foad; Pakizeh, Majid

    2014-05-01

    Kinetics and thermodynamics of mercury ions sorption onto ZnCl2-MCM-41 sorbent were studied. Several rate models in the form of two main classes of mathematic kinetic models (adsorption reaction models and adsorption diffusion models) were investigated. Pseudo-first-order, pseudo-second-order, Elovich, film and intraparticle diffusion models were used to analyze the kinetic data. Results showed that the pseudo-second order model can well describe the adsorption kinetic data. The thermodynamic parameters, such as Gibb's free energy change (ΔG°), standard enthalpy change (ΔH°) and standard entropy change (ΔS°) were also evaluated. Negative value of free energy at temperature range of 20-55 °C, indicates the spontaneous nature of Hg(II) sorption by ZnCl2-MCM-41 sorbent. The adsorption capacity which was found to decrease with temperature showed the exothermic nature of the mercury sorption process (ΔH° = -49.4 kJ mol-1). The negative ΔS° value (-148.9 J mol-1 K-1) revealed a decrease in the randomness at the solid/solution interface and also indicated the fast adsorption of the Hg(II) onto active sites.

  15. Mercury(5)

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    26. Mercury appears to have a center of iron thattakes up seventy-five percent 0f the planet. There isonly a thin outer covering of rock around the core. Someastronomers think most of Mercury's rock was explodedoff when the planet was hit by a huge object early in itshistory.

  16. REMOVAL OF MERCURY FROM WATER USING POLYPYRROLE AND ITS COMPOSITES

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    One of the suitable methods for removing heavy metals from water is by using surface adsorption process. In this paper, the preparation of polypyrrole and its composites as adsorbents are discussed and the capability of separating mercury from water is investigated. The results indicated that the polypyrrole and its composites are able to remove mercury from aqueous media. Furthermore the adsorption percentage is related to the surface morphology, type of additives and its concentration.

  17. Phosphorous adsorption capacity of different substrates and its application to surface flow constructed wetlands%不同基质磷吸附性能及其在表流人工湿地中应用

    Institute of Scientific and Technical Information of China (English)

    熊家晴; 孙璐杨; 陈浩; 王晓昌; 郑于聪; 葛媛

    2015-01-01

    选用煤渣和沙子两种基质进行等温吸附和吸附动力学试验,并结合表面流人工湿地处理含磷废水的效果,研究了煤渣和沙子对磷的吸附特性以及两种基质在表面流湿地中的除磷效果。结果表明:吸附实验中, Freundlich和Langmuir方程均能较好地拟合两种基质对磷的吸附特性,一级反应动力学方程能够很好拟合沙子的吸附动力学曲线,煤渣的动力学拟合情况较差。以煤渣为基质的表面流人工湿地对磷的平均去除率(35.79%)低于以沙子为基质的表面流人工湿地对磷的平均去除率(48.25%),并且沙子湿地除磷的稳定性好于煤渣湿地。%Tests on isothermal adsorption and adsorption kinetics have been conducted with two kinds of substrates:coal cinder and sands. Combined with the effect of surface flow constructed wetland on the treatment of phosphorus-containing wastewater,the adsorbing capacity of coal cinder and sands for phosphorus,and the phosphorus removing effect of the two kinds of substrates in surface flow constructed wetland are studied. The results show that based on ad-sorption tests,both Freundlich and Langmuir equation are well fitted for the adsorption characteristics of the two kinds of substrates for phosphorus. The first-order kinetics equation can be well fitted for the adsorption kinetic curve of sands,but not so well fitted for that of coal cinder. The phosphorus removing rate by coal cinder-substrate surface flow constructed wetland(35.79%) is lower than that by using sand-substrate surface flow con-structed wetland(48.25%). Furthermore,the stability of phosphorus removing capacity of sands wetland is better than that of coal cinder wetland.

  18. Methane adsorption capacity of extracted coals under control of solvent polarity%溶剂极性控制下的煤抽余物吸附甲烷能力研究

    Institute of Scientific and Technical Information of China (English)

    陈润; 王治洋; 秦勇; 王琳琳; 韦重韬; 王优阳

    2015-01-01

    Based upon isothermal methane adsorption on raw and solvent extracted coals, relationship between solvent polarity and methane adsorption capacity change of the coal was analyzed, and the possible geochemical mechanism was discussed from polarity of the solvents. The results show that methane isothermal adsorption curves on the extracted coals follow the Langmuir equation. Extraction with CS2 and C6 H6 enhances methane adsorption capacities on extracted coals, and that with tetrahydrofuran ( THF) and acetone is opposite. There is a negative correlation between methane adsorption capacity change of the coal and the solvent polarity, which can be explained by similarity-intermiscibility theory. The polarities of CS2 and C6 H6 are weaker, which can extract more alkane and aromatic hydrocarbons with nonpolar molecule structure (-CH3 and -CH2-) to increase the adsorbed space of coal surface for methane adsorption. The polarities of THF and acetone are stronger, which can extract more non-hydrocarbon and asphaltene with polar molecule structure (-CHO, -OH and -COOH) to reduce the adsorbed space of coal surface for methane adsorption.%基于原煤和有机溶剂抽余物的等温吸附实验结果,对比分析溶剂极性与其煤抽余物吸附甲烷能力变化关系,探讨抽提溶剂极性差异对煤抽余物吸附甲烷能力控制的地球化学机理。结果表明,煤溶剂抽余物等温吸附甲烷曲线都遵循Langmuir方程,且二硫化碳( CS2)和苯( C6 H6)溶剂抽提作用增大了煤吸附甲烷量,四氢呋喃( THF)和丙酮溶剂抽提作用减小了煤吸附甲烷量。实验发现,煤抽余物吸附甲烷能力变化与抽提溶剂极性成负相关关系,该现象可用相似相容原理解释:CS2和C6 H6溶剂极性较弱,抽提出较多具有非极性结构(-CH3和-CH2-)的烷烃和芳烃,为甲烷在煤表面吸附增多了吸附位而增强了抽余物吸附甲烷能力,THF和丙酮溶剂极性较强,抽提出较

  19. Mercury capture in bench-scale absorbers

    Energy Technology Data Exchange (ETDEWEB)

    Livengood, C.D.; Huang, H.S.; Mendelsohn, M.H.; Wu, J.M.

    1994-08-01

    This paper gives,a brief overview of research being conducted at Argonne National Laboratory on the capture of mercury by both dry sorbents and wet scrubbers. The emphasis in the research is on development of a better understanding of the key factors that control the capture of mercury. Future work is expected to utilize that information for the development of new or modified process concepts featuring enhanced mercury capture capabilities. The results and conclusions to date from the Argonne -research on dry sorbents can be summarized as follows: lime hydrates, either regular or high-surface-area, are `not effective in removing mercury; mercury removals are enhanced by the addition of activated carbon; mercury removals with activated carbon decrease with increasing temperature, larger particle size, and decreasing mercury concentration in the gas; and chemical pretreatment (e.g., with sulfur or (CaCl{sub 2}) can greatly increase the removal capacity of activated carbon. Preliminary results from the wet scrubbing research include: no removal of elemental mercury is obtained under normal scrubber operating conditions; mercury removal is improved by the addition of packing or production of smaller gas bubbles to increase the gas-liquid contact area; polysulfide solutions do not appear promising for enhancing mercury removal in typical FGC systems; stainless steel packing appears to have beneficial properties for mercury removal and should be investigated further; and other chemical additives may offer greatly enhanced removals.

  20. Biochar from malt spent rootlets for the removal of mercury from aqueous solutions

    Science.gov (United States)

    Boutsika, Lamprini; Manariotis, Ioannis; Karapanagioti, Hrissi K.

    2013-04-01

    Biochar is receiving increased attention as a promising material in environmental applications. It is obtained from the incomplete combustion of carbon-rich biomass under oxygen-limited conditions. One of the many proposed applications of biochars is the removal of metals (e.g., lead, mercury, etc.) from aqueous solutions. Mercury is one of the heavy metals of particular concern due to its toxicity even at relatively low concentration and thus, its removal from aqueous systems is desirable. Malt spent rootlets is a by-product formed during beer production, it is inexpensive and it is produced in high quantities. The objective of the present study was to evaluate the potential use of biochar, produced from malt spent rootlets, to remove mercury from aqueous solutions. Batch experiments were conducted at room temperature (25oC) to obtain the optimum sorption conditions under different pH values, biomass dose, contact time, and solution ionic strength. Sorption kinetics and equilibrium capacity constants were determined at the optimum pH value. Furthermore, the effect of different leaching solutions on mercury desorption from the biochar was examined. All studies with mercury and biochar were conducted at pH 5 that was determined to be the optimum pH for sorption. The proportion of mercury removal increased with the increased dose of the biochar, i.e. from 71% removal for biochar dose of 0.3 g/L, it reached almost 100% removal for biochar dose ˜1 g/L. Based on the isotherm data, the maximum biochar sorption capacity (qmax) for mercury was 99 mg/g. Based on the sorption kinetic data, (qmax) was achieved after 2 h; it should be mentioned that 30% of the (qmax) was observed within the first 5 min. Five leaching solutions were tested for mercury desorption (H2O, HCl, EDTA, NaCl and HNO3). HCl resulted in the highest extraction percentage of the sorbed mercury. The desorbing mercury percentages at 24 h for HCl concentrations 0.1, 0.2, 0.4, 0.8, and 2 M were 62, 59, 62, 69

  1. Micromechanism of sulfurizing activated carbon and its ability to adsorb mercury

    Science.gov (United States)

    Wu, Guofang; Xu, Minren; Liu, Qingcai; Yang, Jian; Ma, Dongran; Lu, Cunfang; Lan, Yuanpei

    2013-11-01

    To eliminate mercury from coal-fired flue gas, sulfurization of carbons has been found to be the most inexpensive approach to solve the problem of environment contamination by mercury. This study focuses on improving the adsorption capacity of activate carbon loaded with elemental sulfur as an active phase and further use in the removal of mercury vapors from fuel gas. In this paper, equipment such as the scanning electron microscope, specific surface area test machine and fluorescence spectrophotometer are employed to study the ability of the S-loaded activated carbon. The results show that unmodified activate carbon has smooth hole surface and uneven distributed hole size. Pore walls of activate carbon modified became rougher and the hole size distribution is asymmetrical. Sulfur is uniformly distributed and is mainly bonded on the surface of the skeleton of activate carbon. In addition, a small amount of granular sulfur was loaded on the surface of the pore walls. Higher temperature creates smaller pore size and larger microporous volume. Improving the process temperature is conducive to the development of micropore and the distribution of sulfur, and a larger amount of small molecular weight sulfur are created, which is helpful in the removal of HgO through chemical adsorption. The optimum modification temperature and holding time is 550 °C and 60 min, which creates the adsorbents of the max absorption capability of 1227.5 μg Hg/g.

  2. Phosphorus Adsorption Capacities and Mechanisms of Different Modified Kaolin in Wastewater%改性高岭土对废水中磷的吸附性能及机理研究

    Institute of Scientific and Technical Information of China (English)

    翟由涛; 杭小帅; 干方群

    2012-01-01

    采用盐酸和煅烧2种方法对苏州高岭土进行了改性,分析其对模拟含磷废水中磷的吸附效果,并初步探讨了其作用机制,继而进行了等温吸附和吸附动力学试验研究.结果显示,酸、热改性均不同程度地提高了高岭土对模拟废水中磷的吸附净化能力,尤以9%酸改性和500℃煅烧效果最为明显.在处理25 ml浓度为20 mg/L的模拟含磷废水中,高岭土投加量为2%(重量比)时,经9%酸改性高岭土对磷去除率达81.8%,较天然高岭土提高了44.6%.在处理50 ml浓度为20 mg/L的模拟含磷废水时,经500℃煅烧改性高岭土对磷的去除率高达99.5%,残留溶液中磷浓度仅为0.10 mg/L,达到我国相应排放标准.酸改性可通过改变高岭土的吸附活性点位来提高其对磷的吸附净化性能,而煅烧通过活化高岭石中的铝而提高其对磷的吸附净化性能.天然、9%酸改性及500℃煅烧高岭土磷吸附等温线均符合Freundilch和Langmuir方程,皆达极显著水平(P<0.01).天然、9%酸改性及500℃煅烧高岭土对磷的动力学吸附特征一致,皆与准二级方程拟合最佳,达极显著水平(P<0.01).500℃煅烧高岭土对磷的饱和吸附量最大,征净化含磷废水中具有良好的应用前景.%This study, by modifing kaolin with different concentrations of hydrochloric acid and different temperatures of calcinations, studied the adsorption capacities and mechanisms of phosphorus (P) in synthetic wastewater by the modified kaolin as well as P adsorption isotherms and kinetics of modified kaolin. The results showed that P adsorption capacities of kaolin with hydrochloric acid and calcination in synthetic wastewater were improved differently. Particularly, the adsorption capacities of kaolin modified with 9% acid and 500℃ calcinations improved greatly. The removal capacity of 9% acid modification raised by 44.6% than the capacity of natural kaolin, enabling kaolin, applied at a rate of

  3. Experimental study on fly ash capture mercury in flue gas

    Institute of Scientific and Technical Information of China (English)

    Mercedes; DíAZ-SOMOANO; Patricia; ABAD-VALLE; M.Rosa; MARTíNEZ-TARAZONA

    2010-01-01

    Systematic experiments were conducted on a fixed-bed reactor to investigate the interaction between fly ash and mercury,the results implied that fly ash can capture mercury effectively.Among different fly ashes,the unburned carbon in the FA2 and FA3 fly ashes has the highest mercury capture capacity,up to 10.3 and 9.36 μg/g,respectively,which is close to that of commercial activated carbon.There is no obvious relationship between mercury content and carbon content or BET surface area of fly ash.Petrography classification standard was applied to distinguish fly ash carbon particles.Carbon content is not the only variable that controls mercury capture on fly ash,there are likely significant differences in the mercury capture capacities of the various carbon forms.Mercury capture capacity mainly depends on the content of anisotropy carbon particles with porous network structure.

  4. Mercury and Pregnancy

    Science.gov (United States)

    ... Home > Pregnancy > Is it safe? > Mercury and pregnancy Mercury and pregnancy E-mail to a friend Please ... vision problems. How can you be exposed to mercury? Mercury has several forms: It can be a ...

  5. Biosorption of mercury by Macrocystis pyrifera and Undaria pinnatifida: Influence of zinc, cadmium and nickel

    Institute of Scientific and Technical Information of China (English)

    Josefina Plaza; Marisa Viera; Edgardo Donati; Eric Guibal

    2011-01-01

    This study investigated the adsorption of Hg(Ⅱ) on Macrocystis pyrifera and Undaria pinnatifida in monometallic system in the presence of Zn(Ⅱ),Cd(Ⅱ) and Ni(Ⅱ).The two biosorbents reached the same maximum sorption capacity (qm =0.8 mmol/g) for mercury.U.pinnatifida showed a greater affinity (given by the coefficient b of the Langmuir equation) for mercury compared to M.pyrifera (4.4 versus 2.7 L/mmol).Mercury uptake was significantly reduced (by more than 50%) in the presence of competitor heavy metals such as Zn(Ⅱ),Cd(Ⅱ) and Ni(Ⅱ).Samples analysis using an environmental scanning electron microscopy equipped with an energy dispersive X-ray microanalysis showed that mercury was heterogeneously adsorbed on the surface of both biomaterials,while the other heavy metals were homogeneous distributed.The analysis of biosorbents by Fourier transform infrared spectrometry indicated that Hg(Ⅱ)binding occurred on S=O (sulfonate) and N-H (amine) functional groups.

  6. Determination of binding capacity and adsorption enthalpy between Human Glutamate Receptor (GluR1) peptide fragments and kynurenic acid by surface plasmon resonance experiments.

    Science.gov (United States)

    Csapó, E; Majláth, Z; Juhász, Á; Roósz, B; Hetényi, A; Tóth, G K; Tajti, J; Vécsei, L; Dékány, I

    2014-11-01

    The interaction between kynurenic acid (KYNA) and two peptide fragments (ca. 30 residues) of Human Glutamate Receptor 201-300 (GluR1) using surface plasmon resonance (SPR) spectroscopy was investigated. Because of the medical interest in the neuroscience, GluR1 is one of the important subunits of the α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPAR). AMPARs are ionotoropic glutamate receptors, which are mediating fast synaptic transmission and are crucial for plasticity in the brain. On the other hand, KYNA has been suggested to have neuroprotective activity and it has been considered for apply in therapy in certain neurobiological disorders. In this article the adsorption of the GluR1201-230 and GluR1231-259 peptides were studied on gold biosensor chip. The peptides were chemically bonded onto the gold surface via thiol group of L-cysteine resulted in the formation of peptide monolayer on the SPR chip surface. Because the GluR1231-259 peptide does not contain L-cysteine the Val256 was replaced by Cys256. The cross sectional area and the surface orientation of the studied peptides were determined by SPR and theoretical calculations (LOMETS) as well. The binding capability of KYNA on the peptide monolayer was studied in the concentration range of 0.1-5.0 mM using 150 mM NaCl ionic strength at pH 7.4 (±0.02) in phosphate buffer solutions. In order to determine the binding enthalpy the experiments were carried out between +10°C and +40°C. The heat of adsorption was calculated by using adsorption isotherms at different surface loading of KYNA on the SPR chip.

  7. Preparation and Characterization of Ni-Doped Calcium Silicate Hydrate Based on Steel Slag: Adsorption Capacity for Rhodamine B from Aqueous Solution

    OpenAIRE

    2015-01-01

    Calcium silicate hydrate based on steel slag (SCSH) and Ni-doped SCSH (NSCSH) were synthesized under specific hydrothermal conditions at saturated vapor pressure and 185°C for 7 hours. The structure and morphology of SCSH and NSCSH were characterized by XRD, SEM, and N2 adsorption/desorption. SCSH mainly consisted of amorphous calcium silicate hydrate gel (C-S-H gel) together with some flake-like tobermorite and NSCSH consisted of crystalline tobermorite and xonotlite. The addition of Ni(NO3)...

  8. Influence of fixed carbon on coal textural character and methane adsorption capacity%固定碳对煤的孔结构和甲烷吸附量的影响

    Institute of Scientific and Technical Information of China (English)

    郝世雄; 王承洋; 江成发

    2012-01-01

    Four kinds of coal with different fixed carbon content were selected as experimental samples. The sur- face morphology and textural character of the samples were characterized by scanning electron microscope ( SEM), N2 adsorption-desorption at 77 K, respectively, and their specific surface, pore volume and pore-size distribution were cal- culated based on N2 adsorption-desorption isotherms. And the volumetric method was used to determine its performance of methane adsorption. The influences of fixed carbon content on coal surface morphology, specific surface area, pore volume, pore size distribution and methane sorption capacity were discussed. The results show that fixed carbon con- tent has little influence on specific surface area, pore volume, and pore size distribution when fixed carbon content is in the range of 70.17% -88.34%. When fixed carbon content changes from 88.34% to 94.45% , coal specific surface area and mieropore volume increases 1.84 and 5.06 times respectively, and the pore size distribution moves to micro- pore. Methane adsorption capacity follows a U shape second-order polynomial trend with fixed carbon content.%以4种不同固定碳质量分数的煤样作为研究对象,采用SEM表征其形貌,采用77 K时的N2吸脱附实验测定其比表面积、孔容和孔径分布,容量法测定其吸附甲烷的性能,并讨论煤的固定碳质量分数对其比表面积、孔容和吸附甲烷能力的影响。结果表明:当固定碳质量分数从70.17%增大到88.34%时,固定碳质量分数对煤的表面形貌、比表面积、孔容以及孔径分布的影响不显著;当固定碳质量分数从88.34%增大到94.45%时,煤的比表面积、微孔孔容分别增大1.84倍和5.06倍,孔径分布向微孔方向移动;Langmuir体积VL与固定碳质量分数(70.17%~94.45%)呈U型的二次多项式关系。

  9. Removal of heavy metals from water by zeolite mineral chemically modified. Mercury as a particular case

    International Nuclear Information System (INIS)

    Research works on the removal of mercury from water by zeolite minerals show that a small quantity of this element is sorbed. In this work the mercury sorption from aqueous solutions in the presence and absence of Cu(l l), Ni(l l) and/or Zn(l l) by a Mexican zeolite mineral, natural and modified by cisteaminium chloride or cistaminium dichloride, was investigated in acidic p H. The zeolite minerals were characterized by X- Ray diffraction Ftir, scanning electron microscopy and semiquantitative elemental analysis (EDS), surface area analysis (BET) and thermogravimetric analysis (TGA). Mercury from aqueous solutions was quantified by Atomic absorption spectroscopy. The amount of sulphur on the zeolite samples treated with Na CI and modified with cisteaminium chloride (0.375 mmol/g) or cistaminium dichloride(0.475 mmol/g) was found to be higher than that of the zeolite minerals modified with cisteaminium chloride and cistaminium dichloride without treating them with Na CI. The amount of sulphur on the zeolite minerals modified with thiourea was the lowest. The diffusion coefficients and sorption isotherms for mercury were determined in the natural, treated with Na CI and, treated with Na CI and then modified with the cisteaminium chloride or cistaminium dichloride zeolite samples. The retention of mercury was the highest for the zeolite minerals treated Na CI and then modified with cisteaminium chloride or cistaminium dichloride, with adsorption capacity of 0.0511 and 0.0525 mmol Hg/g, respectively. In this research work, it was found that the retention of mercury by the modified minerals was not affected by the presence of Cu (Il), Zn(l l) y Ni (I l) under the experimental conditions. (Author)

  10. Got Mercury?

    Science.gov (United States)

    Meyers, Valerie; James, John T.; McCoy, Torin; Garcia, Hector

    2010-01-01

    Many lamps used in various spacecraft contain elemental mercury, which is efficiently absorbed through the lungs as a vapor. The liquid metal vaporizes slowly at room temperature, but may be completely vaporized when lamps are operating. Because current spacecraft environmental control systems are unable to remove mercury vapors, we considered short-term and long-term exposures. Using an existing study, we estimated mercury vapor releases from lamps that are not in operation during missions lasting less than or equal to 30 days; whereas we conservatively assumed complete vaporization from lamps that are operating or being used during missions lasing more than 30 days. Based on mercury toxicity, the Johnson Space Center's Toxicology Group recommends stringent safety controls and verifications for any hardware containing elemental mercury that could yield airborne mercury vapor concentrations greater than 0.1 mg/m3 in the total spacecraft atmosphere for exposures lasting less than or equal to 30 days, or concentrations greater than 0.01 mg/m3 for exposures lasting more than 30 days.

  11. Preparation of char from lotus seed biomass and the exploration of its dye removal capacity through batch and column adsorption studies.

    Science.gov (United States)

    Nethaji, S; Sivasamy, A; Kumar, R Vimal; Mandal, A B

    2013-06-01

    Char was obtained from lotus seed biomass by a simple single-step acid treatment process. It was used as an adsorbent for the removal of malachite green dye (MG) from simulated dye bath effluent. The adsorbent was characterized for its surface morphology, surface functionalities, and zero point charge. Batch studies were carried out by varying the parameters such as initial aqueous pH, adsorbent dosage, adsorbent particle size, and initial adsorbate concentration. Langmuir and Freundlich isotherms were used to test the isotherm data and the Freundlich isotherm best fitted the data. Thermodynamic studies were carried out and the thermodynamic parameters such as ∆G, ∆H, and ∆S were evaluated. Adsorption kinetics was carried out and the data were tested with pseudofirst-order model, pseudosecond-order model, and intraparticle diffusion model. Adsorption of MG was not solely by intraparticle diffusion but film diffusion also played a major role. Continuous column experiments were also conducted using microcolumn and the spent adsorbent was regenerated using ethanol and was repeatedly used for three cycles in the column to determine the reusability of the regenerated adsorbent. The column data were modeled with the modeling equations such as Adam-Bohart model, Bed Depth Service Time (BDST) model, and Yoon-Nelson model for all the three cycles.

  12. Preparation of Graphene Oxide Decorated Fe3O4@SiO2 Nanocomposites with Superior Adsorption Capacity and SERS Detection for Organic Dyes

    Directory of Open Access Journals (Sweden)

    Song Yang

    2015-01-01

    Full Text Available The fast detection and removal of organic dyes from contaminated water has become an urgent environmental issue due to their high toxicity, chemical stability, and low biodegradability. In this paper, we have developed graphene oxide decorated Fe3O4@SiO2 (Fe3O4@SiO2-GO as a novel adsorbent aiming at the rapid adsorption and trace analysis of organic dyes followed by surface enhanced Raman scattering (SERS. The structure and morphology of the nanocomposites were characterized by transmission electron microscopy (TEM, Fourier infrared spectrometry (FT-IR, X-ray diffraction (XRD, and vibrating sample magnetometer (VSM. The obtained nanocomposites were used to adsorb methylene blue (MB in aqueous solution based on π-π stacking interaction and electrostatic attraction between MB and GO, and the adsorption behaviors of MB were investigated. Moreover, the obtained nanocomposites with adsorbed dyes were separated from the solution and loaded with silver nanoparticles for SERS detection. These nanocomposites showed superior SERS sensitivity and the lowest detectable concentration was 1.0 × 10−7 M.

  13. Adsorption in air treatment; Adsorption en traitement de l'air

    Energy Technology Data Exchange (ETDEWEB)

    Le Cloirec, P. [Ecole des Mines de Nantes, Dept. Systemes Energetiques et Environnement, 44 - Nantes (France)

    2003-01-01

    The aim of this article is to present the concepts and technologies of adsorption in air treatment. The following points are more particularly developed: 1 - approach of mechanisms: gas-solid transfer, equilibrium equations, multi-composed adsorption, adsorption influencing parameters, adsorption-desorption capacities and energies, specific case of hydrogen sulfide, the case of ketones; 2 - adsorbents implemented; 3 - adsorption and dynamical adsorber: flow and pressure drop in a porous medium, breakthrough curves, adsorption capacities, modeling of breakthrough curves; 4 - implementation of adsorber: models, dimensioning and practical operating data, process safety; 5 - regeneration of activated charcoals: reactivation, in-situ thermal regeneration. (J.S.)

  14. Mercury(II) and methyl mercury speciation on Streptococcus pyogenes loaded Dowex Optipore SD-2

    Energy Technology Data Exchange (ETDEWEB)

    Tuzen, Mustafa, E-mail: m.tuzen@gmail.com [Gaziosmanpasa University, Faculty of Science and Arts, Chemistry Department, 60250 Tokat (Turkey); Uluozlu, Ozgur Dogan [Gaziosmanpasa University, Faculty of Science and Arts, Chemistry Department, 60250 Tokat (Turkey); Karaman, Isa [Gaziosmanpasa University, Faculty of Science and Arts, Biology Department, 60250 Tokat (Turkey); Soylak, Mustafa [Erciyes University, Faculty of Science and Arts, Chemistry Department, 38039 Kayseri (Turkey)

    2009-09-30

    A solid phase extraction procedure based on speciation of mercury(II) and methyl mercury on Streptococcus pyogenes immobilized on Dowex Optipore SD-2 has been established. Selective and sequential elution with 0.1 mol L{sup -1} HCl for methyl mercury and 2 mol L{sup -1} HCl for mercury(II) were performed at pH 8. The determination of mercury levels was performed by cold vapour atomic absorption spectrometry (CVAAS). Optimal analytical conditions including pH, amounts of biosorbent, sample volumes, etc., were investigated. The influences of the some alkaline and earth alkaline ions and some transition metals on the recoveries were also investigated. The capacity of biosorbent for mercury(II) and methyl mercury was 4.8 and 3.4 mg g{sup -1}. The detection limit (3 sigma) of the reagent blank for mercury(II) and methyl mercury was 2.1 and 1.5 ng L{sup -1}. Preconcentration factor was calculated as 25. The relative standard deviations of the procedure were below 7%. The validation of the presented procedure is performed by the analysis of standard reference material (NRCC-DORM 2 Dogfish Muscle). The procedure was successfully applied to the speciation of mercury(II) and methyl mercury in natural water and environmental samples.

  15. Mercury(II) and methyl mercury speciation on Streptococcus pyogenes loaded Dowex Optipore SD-2.

    Science.gov (United States)

    Tuzen, Mustafa; Uluozlu, Ozgur Dogan; Karaman, Isa; Soylak, Mustafa

    2009-09-30

    A solid phase extraction procedure based on speciation of mercury(II) and methyl mercury on Streptococcus pyogenes immobilized on Dowex Optipore SD-2 has been established. Selective and sequential elution with 0.1 mol L(-1) HCl for methyl mercury and 2 mol L(-1) HCl for mercury(II) were performed at pH 8. The determination of mercury levels was performed by cold vapour atomic absorption spectrometry (CVAAS). Optimal analytical conditions including pH, amounts of biosorbent, sample volumes, etc., were investigated. The influences of the some alkaline and earth alkaline ions and some transition metals on the recoveries were also investigated. The capacity of biosorbent for mercury(II) and methyl mercury was 4.8 and 3.4 mg g(-1). The detection limit (3 sigma) of the reagent blank for mercury(II) and methyl mercury was 2.1 and 1.5 ng L(-1). Preconcentration factor was calculated as 25. The relative standard deviations of the procedure were below 7%. The validation of the presented procedure is performed by the analysis of standard reference material (NRCC-DORM 2 Dogfish Muscle). The procedure was successfully applied to the speciation of mercury(II) and methyl mercury in natural water and environmental samples.

  16. Expanded bed adsorption of bromelain (E.C. 3.4.22.33) from Ananas comosus crude extract

    OpenAIRE

    Silveira, E.; M. E. Souza-Jr; J. C. C. Santana; A. C. Chaves; L. F. Porto; E. B. Tambourgi

    2009-01-01

    This work focuses on the adsorption of Bromelain in expanded bed conditions, such as the adsorption kinetics parameters. The adsorption kinetics parameters showed that after 40 minutes equilibrium was achieved and maximum adsorption capacity was 6.11 U per resin mL. However, the maximum adsorption capacity was only determined by measuring the adsorption isotherm. Only by the Langmuir model the maximum adsorption capacity, Qm, and dissociation constant, kd, values could be estimated as 9.18 U/...

  17. Oxidation of Mercury in Products of Coal Combustion

    Energy Technology Data Exchange (ETDEWEB)

    Peter Walsh; Giang Tong; Neeles Bhopatkar; Thomas Gale; George Blankenship; Conrad Ingram; Selasi Blavo Tesfamariam Mehreteab; Victor Banjoko; Yohannes Ghirmazion; Heng Ban; April Sibley

    2009-09-14

    Laboratory measurements of mercury oxidation during selective catalytic reduction (SCR) of nitric oxide, simulation of pilot-scale measurements of mercury oxidation and adsorption by unburned carbon and fly ash, and synthesis of new materials for simultaneous oxidation and adsorption of mercury, were performed in support of the development of technology for control of mercury emissions from coal-fired boilers and furnaces. Conversion of gas-phase mercury from the elemental state to water-soluble oxidized form (HgCl{sub 2}) enables removal of mercury during wet flue gas desulfurization. The increase in mercury oxidation in a monolithic V{sub 2}O{sub 5}-WO{sub 3}/TiO{sub 2} SCR catalyst with increasing HCl at low levels of HCl (< 10 ppmv) and decrease in mercury oxidation with increasing NH{sub 3}/NO ratio during SCR were consistent with results of previous work by others. The most significant finding of the present work was the inhibition of mercury oxidation in the presence of CO during SCR of NO at low levels of HCl. In the presence of 2 ppmv HCl, expected in combustion products from some Powder River Basin coals, an increase in CO from 0 to 50 ppmv reduced the extent of mercury oxidation from 24 {+-} 3 to 1 {+-} 4%. Further increase in CO to 100 ppmv completely suppressed mercury oxidation. In the presence of 11-12 ppmv HCl, increasing CO from 0 to {approx}120 ppmv reduced mercury oxidation from {approx}70% to 50%. Conversion of SO{sub 2} to sulfate also decreased with increasing NH{sub 3}/NO ratio, but the effects of HCl and CO in flue gas on SO{sub 2} oxidation were unclear. Oxidation and adsorption of mercury by unburned carbon and fly ash enables mercury removal in a particulate control device. A chemical kinetic mechanism consisting of nine homogeneous and heterogeneous reactions for mercury oxidation and removal was developed to interpret pilot-scale measurements of mercury oxidation and adsorption by unburned carbon and fly ash in experiments at pilot

  18. Mercury removal from coal combustion flue gas by modified fly ash.

    Science.gov (United States)

    Xu, Wenqing; Wang, Hairui; Zhu, Tingyu; Kuang, Junyan; Jing, Pengfei

    2013-02-01

    Fly ash is a potential alternative to activated carbon for mercury adsorption. The effects of physicochemical properties on the mercury adsorption performance of three fly ash samples were investigated. X-ray fluorescence spectroscopy, X-ray photoelectron spectroscopy, and other methods were used to characterize the samples. Results indicate that mercury adsorption on fly ash is primarily physisorption and chemisorption. High specific surface areas and small pore diameters are beneficial to efficient mercury removal. Incompletely burned carbon is also an important factor for the improvement of mercury removal efficiency, in particular. The C-M bond, which is formed by the reaction of C and Ti, Si and other elements, may improve mercury oxidation. The samples modified with CuBr2, CuCl2 and FeCl3 showed excellent performance for Hg removal, because the chlorine in metal chlorides acts as an oxidant that promotes the conversion of elemental mercury (Hg0) into its oxidized form (Hg2+). Cu2+ and Fe3+ can also promote Hg0 oxidation as catalysts. HCl and O2 promote the adsorption of Hg by modified fly ash, whereas SO2 inhibits the Hg adsorption because of competitive adsorption for active sites. Fly ash samples modified with CuBr2, CuCl2 and FeCl3 are therefore promising materials for controlling mercury emissions. PMID:23596961

  19. Mercury removal from coal combustion flue gas by modified fly ash

    Institute of Scientific and Technical Information of China (English)

    Wenqing Xu; Hairui Wang; Tingyu Zhu; Junyan Kuang; Pengfei Jing

    2013-01-01

    Fly ash is a potential alternative to activated carbon for mercury adsorption.The effects of physicochemical properties on the mercury adsorption performance of three fly ash samples were investigated.X-ray fluorescence spectroscopy,X-ray photoelectron spectroscopy,and other methods were used to characterize the samples.Results indicate that mercury adsorption on fly ash is primarily physisorption and chemisorption.High specific surface areas and small pore diameters are beneficial to efficient mercury removal.Incompletely burned carbon is also an important factor for the improvement of mercury removal efficiency,in particular.The C-M bond,which is formed by the reaction of C and Ti,Si and other elements,may improve mercury oxidation.The samples modified with CuBr2,CuCl2 and FeCl3 showed excellent performance for Hg removal,because the chlorine in metal chlorides acts as an oxidant that promotes the conversion of elemental mercury (Hg0) into its oxidized form (Hg2+).Cu2+ and Fe3+ can also promote Hg0 oxidation as catalysts.HCland O2 promote the adsorption of Hg by modified fly ash,whereas SO2 inhibits the Hg adsorption because of competitive adsorption for active sites.Fly ash samples modified with CuBr2,CuCl2 and FeCl3 are therefore promising materials for controlling mercury emissions.

  20. Mercury and autism: accelerating evidence?

    Science.gov (United States)

    Mutter, Joachim; Naumann, Johannes; Schneider, Rainer; Walach, Harald; Haley, Boyd

    2005-10-01

    The causes of autism and neurodevelopmental disorders are unknown. Genetic and environmental risk factors seem to be involved. Because of an observed increase in autism in the last decades, which parallels cumulative mercury exposure, it was proposed that autism may be in part caused by mercury. We review the evidence for this proposal. Several epidemiological studies failed to find a correlation between mercury exposure through thimerosal, a preservative used in vaccines, and the risk of autism. Recently, it was found that autistic children had a higher mercury exposure during pregnancy due to maternal dental amalgam and thimerosal-containing immunoglobulin shots. It was hypothesized that children with autism have a decreased detoxification capacity due to genetic polymorphism. In vitro, mercury and thimerosal in levels found several days after vaccination inhibit methionine synthetase (MS) by 50%. Normal function of MS is crucial in biochemical steps necessary for brain development, attention and production of glutathione, an important antioxidative and detoxifying agent. Repetitive doses of thimerosal leads to neurobehavioral deteriorations in autoimmune susceptible mice, increased oxidative stress and decreased intracellular levels of glutathione in vitro. Subsequently, autistic children have significantly decreased level of reduced glutathione. Promising treatments of autism involve detoxification of mercury, and supplementation of deficient metabolites.

  1. Bone char surface modification by nano-gold coating for elemental mercury vapor removal

    Energy Technology Data Exchange (ETDEWEB)

    Assari, Mohamad javad [Department of Environmental & Occupational Health, Faculty of Medical Sciences, Tarbiat Modares university, Tehran (Iran, Islamic Republic of); Rezaee, Abbas, E-mail: rezaee@modares.ac.ir [Department of Environmental & Occupational Health, Faculty of Medical Sciences, Tarbiat Modares university, Tehran (Iran, Islamic Republic of); Rangkooy, Hossinali [Occupational Health Department, Faculty of Health, Jondishapor Medical Sciences University, Ahvaz (Iran, Islamic Republic of)

    2015-07-01

    Highlights: • A novel nanocomposite including bone char and gold nanoparticle was developed for capture of Hg{sup 0} vapor. • EDS and XRD results confirm the presence of nano-gold on the surface of the bone char support. • The majority of the pores were found to be in the mesoporous range. • The dynamic capacity of 586 μg/g was obtained for Hg{sup 0} vapor. - Abstract: The present work was done to develop a novel nanocomposite using bone char coated with nano-gold for capture of elemental mercury (Hg{sup 0}) from air. The morphologies, structures, and chemical constitute of the prepared nanocomposite were evaluated by UV–VIS–NIR, dynamic light-scattering (DLS), X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infra-red (FTIR) spectroscopy, and energy dispersive X-ray spectroscopy (EDS). The capture performance of nanocomposite was evaluated in a needle trap for mercury vapor. An on-line setup based on cold vapor atomic absorption spectrometry (CVAAS) was designed for Hg{sup 0} determination. Dynamic capacity of nanocomposite for Hg{sup 0} was shown high efficient operating capacity of 586.7 μg/g. As temperature increases, the dynamic adsorption capacity of the nanocomposite was decreased, which are characteristics of physicosorption processes. It was found that the surface modification of bone char with nano-gold has various advantages such as high operating dynamic adsorption capacity and low cost preparation. It was also demonstrated that the developed nanocomposite is suitable for on-line monitoring of Hg{sup 0}. It could be applied for the laboratory and field studies.

  2. Bone char surface modification by nano-gold coating for elemental mercury vapor removal

    International Nuclear Information System (INIS)

    Highlights: • A novel nanocomposite including bone char and gold nanoparticle was developed for capture of Hg0 vapor. • EDS and XRD results confirm the presence of nano-gold on the surface of the bone char support. • The majority of the pores were found to be in the mesoporous range. • The dynamic capacity of 586 μg/g was obtained for Hg0 vapor. - Abstract: The present work was done to develop a novel nanocomposite using bone char coated with nano-gold for capture of elemental mercury (Hg0) from air. The morphologies, structures, and chemical constitute of the prepared nanocomposite were evaluated by UV–VIS–NIR, dynamic light-scattering (DLS), X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infra-red (FTIR) spectroscopy, and energy dispersive X-ray spectroscopy (EDS). The capture performance of nanocomposite was evaluated in a needle trap for mercury vapor. An on-line setup based on cold vapor atomic absorption spectrometry (CVAAS) was designed for Hg0 determination. Dynamic capacity of nanocomposite for Hg0 was shown high efficient operating capacity of 586.7 μg/g. As temperature increases, the dynamic adsorption capacity of the nanocomposite was decreased, which are characteristics of physicosorption processes. It was found that the surface modification of bone char with nano-gold has various advantages such as high operating dynamic adsorption capacity and low cost preparation. It was also demonstrated that the developed nanocomposite is suitable for on-line monitoring of Hg0. It could be applied for the laboratory and field studies

  3. JV Task 5 - Evaluation of Residual Oil Fly Ash As A Mercury Sorbent For Coal Combustion Flue Gas

    Energy Technology Data Exchange (ETDEWEB)

    Robert Patton

    2006-12-31

    The mercury adsorption capacity of a residual oil fly ash (ROFA) sample collected form Florida Power and Light Company's Port Everglades Power Plant was evaluated using a bituminous coal combustion flue gas simulator and fixed-bed testing protocol. A size-segregated (>38 {micro}g) fraction of ROFA was ground to a fine powder and brominated to potentially enhance mercury capture. The ROFA and brominated-ROFA were ineffective in capturing or oxidizing the Hg{sup 0} present in a simulated bituminous coal combustion flue gas. In contrast, a commercially available DARCO{reg_sign} FGD initially adsorbed Hg{sup 0} for about an hour and then catalyzed Hg{sup 0} oxidation to produce Hg{sup 2+}. Apparently, the unburned carbon in ROFA needs to be more rigorously activated in order for it to effectively capture and/or oxidize Hg{sup 0}.

  4. Synthesis and characterization of LTA nanozeolite using barley husk silica: Mercury removal from standard and real solutions

    International Nuclear Information System (INIS)

    Highlights: ► Silica extraction from barley husk with high purity for the synthesis of A nanozeolite. ► Free template A nanozeolite synthesized via new source of silica at low temperature. ► Optimization of SiO2/Al2O3, Na2O/SiO2 ratios, temperature and time of the synthesis. ► Utilizing of synthesized A nanozeolite for mercury removal from aqueous solutions. ► Mercury removal at optimized pH, contact time and adsorbent dose from real solution. - Abstract: In this study, synthesized Lined Type A (LTA) nanozeolite from barley husk silica (BHS) was used for mercury removal from standard and real aqueous solutions. The BHS in amorphous phase with 80% purity was extracted from barley husk ash (BHA), and used effectively as a new source of silica for the synthesis of NaA nanozeolite. The NaA nanocrystal in pure phase has been synthesized at low temperature, without adding any organic additives. The effects of heating time, reaction temperature, SiO2/Al2O3, and Na2O/SiO2 mole ratios on the crystallization of NaA nanozeolite were studied. The adsorption capacity of mercury (II) was studied as a function of pH, contact time, and amount of adsorbent. The crystallization of NaA nanozeolite from BHS was characterized by X-ray diffraction (XRD), X-ray fluorescence (XRF), scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), Brunauer–Emmett–Teller (BET), and FTIR techniques. Moreover, concentration of Hg2+ ions in the aqueous solutions was analyzed by hydride generation atomic absorption spectroscopy method (HG-AAS). The standard and real samples analysis showed that NaA nanozeolite is capable of Hg2+ ions removal from the aqueous solutions. Efficiency of mercury (II) adsorption from real solutions onto the nano-sized NaA zeolite was 98%

  5. Mercury in mercury(II)-spiked soils is highly susceptible to plant bioaccumulation.

    Science.gov (United States)

    Hlodák, Michal; Urík, Martin; Matúš, Peter; Kořenková, Lucia

    2016-01-01

    Heavy metal phytotoxicity assessments usually use soluble metal compounds in spiked soils to evaluate metal bioaccumulation, growth inhibition and adverse effects on physiological parameters. However, exampling mercury phytotoxicity for barley (Hordeum vulgare) this paper highlights unsuitability of this experimental approach. Mercury(II) in spiked soils is extremely bioavailable, and there experimentally determined bioaccumulation is significantly higher compared to reported mercury bioaccumulation efficiency from soils collected from mercury-polluted areas. Our results indicate this is not affected by soil sorption capacity, thus soil ageing and formation of more stable mercuric complexes with soil fractions is necessary for reasonable metal phytotoxicity assessments.

  6. Copper adsorption in tropical oxisols

    Directory of Open Access Journals (Sweden)

    Silveira Maria Lucia Azevedo

    2003-01-01

    Full Text Available Cu adsorption, at concentrations between 0 to 800 mg L-1, was evaluated in surface and subsurface samples of three Brazilian soils: a heavy clayey-textured Rhodic Hapludalf (RH, a heavy clayey-textured Anionic ''Rhodic'' Acrudox (RA and a medium-textured Anionic ''Xanthic'' Acrudox (XA. After adsorption, two consecutive extractions were performed to the samples which received 100 mg L-1 copper. Surface samples adsorbed higher amounts of Cu than the subsurface, and exhibited lower Cu removed after the extractions, reinforcing the influence of the organic matter in the reactions. Cu adsorption was significant in the subsurface horizons of the Oxisols, despite the positive balance of charge, demonstrating the existence of mechanisms for specific adsorption, mainly related to the predominance of iron and aluminum oxides in the mineral fractions. In these samples, Cu was easily removed from the adsorption sites. RH demonstrated a higher capacity for the Cu adsorption in both horizons.

  7. DFT study of Hg adsorption on M-substituted Pd(1 1 1) and PdM/γ-Al2O3(1 1 0) (M = Au, Ag, Cu) surfaces

    Science.gov (United States)

    Wang, Jiancheng; Yu, Huafeng; Geng, Lu; Liu, Jianwen; Han, Lina; Chang, Liping; Feng, Gang; Ling, Lixia

    2015-11-01

    The adsorption of Hgn (n = 1-3) on the Au-, Ag-, Cu-substituted Pd(1 1 1) surfaces as well as the PdM/γ-Al2O3(1 1 0) (M = Au, Ag, Cu) surfaces has been investigated using spin-polarized density functional theory calculations. It is found that M-substituted Pd(1 1 1) surfaces show as good Hg adsorption capacity as the perfect Pd(1 1 1) at low Hg coverage, while the Hg adsorption capacity is only slightly weakened at high Hg coverage. On the basis of stepwise adsorption energies analysis, it is concluded that M-substituted Pd(1 1 1) surfaces can contribute to the binding of Hg atom on the surfaces at high Hg coverage. The electronic properties of the second metal atoms are the main factor contributes to the Hg adsorption capacity. Gas phase Pd2 shows better Hg adsorption capacity than Pd2/γ-Al2O3, while PdM/γ-Al2O3 can adsorb Hg more efficiently than bare PdM clusters. It suggests that the γ-Al2O3 support can enhance the activity of PdM for Hg adsorption and reduces the activity of Pd2. It is also found that Pd is the main active composition responsible for the interaction of mercury with the surface for PdM/γ-Al2O3 sorbent. Taking Hg adsorption capacity and economic costs into account, Cu addition is a comparatively good candidate for Hg capture.

  8. Competitive adsorption of heavy metal ions on peat

    Institute of Scientific and Technical Information of China (English)

    LIU Zhi-rong; ZHOU Li-min; WEI Peng; ZENG Kai; WEN Chuan-xi; LAN Hui-hua

    2008-01-01

    The uptake capacities, and the adsorption kinetics, of copper, Cu(Ⅱ), nickel, Ni(Ⅱ), and cadmium, Cd(Ⅱ), on peat have been studied under static conditions. The results show that the adsorption rates are rapid: equilibrium is reached in twenty minutes. The adsorption of copper, nickel and cadmium is pH dependent over the pH range from 2 to 6. The adsorption kinetics can be excellently described by the Elovich kinetic equation. The adsorption isotherm fits a Langmuir model very well. The adsorption capacifies follow the order Cu2+>Ni2+>Cd2+ in single-component systems and the competitive adsorption capacities fall in the decreasing order Cu2+> Ni2+>Cd2+ in multi-component systems. The adsorption capacities of these three heavy metal ions on peat are consistent with their observed competitive adsorption capacities.

  9. Adsorption Characteristics of Remazol Black B on Anoxic Sludge

    Institute of Scientific and Technical Information of China (English)

    HUANG Man-hong; CHEN Liang; CHEN Dong-hui; CHEN Chao-peng

    2009-01-01

    The adsorption characteristics of Remazol Black B on anoxic sludge were investigated. The parameters, such as initial pH, sulphate concentration, and temperature,affecting the dye adsorption were studied. The adsorption data were analyzed with three adsorption isotherm models,namely Langmuir, Freudlich, and linear partition. The results showed that adsorption of Remazol Black B on the sterilized sludge reached equilibrium in 4 h. It also indicated that pH had significant effect on anoxic sludge adsorption behavior. The adsorption capacity of anoxic sludge decreased with the increase of pH value and the maximum adsorption capacity of dyes occurred at pH = 3. The adsorptive capacities increased with the decrease of temperature and increase of sulphate concentration. Results also indicated that the adsorption equilibrium of Remazol Black B on anoxic sludge could be well fitted by Freundlich model.

  10. Sorbents for the oxidation and removal of mercury

    Science.gov (United States)

    Olson, Edwin S.; Holmes, Michael J.; Pavlish, John H.

    2008-10-14

    A promoted activated carbon sorbent is described that is highly effective for the removal of mercury from flue gas streams. The sorbent comprises a new modified carbon form containing reactive forms of halogen and halides. Optional components may be added to increase reactivity and mercury capacity. These may be added directly with the sorbent, or to the flue gas to enhance sorbent performance and/or mercury capture. Mercury removal efficiencies obtained exceed conventional methods. The sorbent can be regenerated and reused. Sorbent treatment and preparation methods are also described. New methods for in-flight preparation, introduction, and control of the active sorbent into the mercury contaminated gas stream are described.

  11. Kinetic and thermodynamic studies of Hg(II) adsorption onto MCM-41 modified by ZnCl{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Raji, Foad; Pakizeh, Majid, E-mail: pakizeh@um.ac.ir

    2014-05-01

    Highlights: • ZnCl{sub 2}-MCM-41 introduced itself as a high performance sorbent for Hg(II) removal. • Kinetics data were analyzed by pseudo-first and second order and diffusion models. • The adsorption kinetic data were described very well by pseudo-second-order model. • Sorption of Hg(II) by ZnCl{sub 2}-MCM-41 was an exothermic chemical process. • Hg(II) sorption was a spontaneous process since of minus free energy change. - Abstract: Kinetics and thermodynamics of mercury ions sorption onto ZnCl{sub 2}-MCM-41 sorbent were studied. Several rate models in the form of two main classes of mathematic kinetic models (adsorption reaction models and adsorption diffusion models) were investigated. Pseudo-first-order, pseudo-second-order, Elovich, film and intraparticle diffusion models were used to analyze the kinetic data. Results showed that the pseudo-second order model can well describe the adsorption kinetic data. The thermodynamic parameters, such as Gibb's free energy change (ΔG°), standard enthalpy change (ΔH°) and standard entropy change (ΔS°) were also evaluated. Negative value of free energy at temperature range of 20–55 °C, indicates the spontaneous nature of Hg(II) sorption by ZnCl{sub 2}-MCM-41 sorbent. The adsorption capacity which was found to decrease with temperature showed the exothermic nature of the mercury sorption process (ΔH° = −49.4 kJ mol{sup −1}). The negative ΔS° value (−148.9 J mol{sup −1} K{sup −1}) revealed a decrease in the randomness at the solid/solution interface and also indicated the fast adsorption of the Hg(II) onto active sites.

  12. Kinetic and thermodynamic studies of Hg(II) adsorption onto MCM-41 modified by ZnCl2

    International Nuclear Information System (INIS)

    Highlights: • ZnCl2-MCM-41 introduced itself as a high performance sorbent for Hg(II) removal. • Kinetics data were analyzed by pseudo-first and second order and diffusion models. • The adsorption kinetic data were described very well by pseudo-second-order model. • Sorption of Hg(II) by ZnCl2-MCM-41 was an exothermic chemical process. • Hg(II) sorption was a spontaneous process since of minus free energy change. - Abstract: Kinetics and thermodynamics of mercury ions sorption onto ZnCl2-MCM-41 sorbent were studied. Several rate models in the form of two main classes of mathematic kinetic models (adsorption reaction models and adsorption diffusion models) were investigated. Pseudo-first-order, pseudo-second-order, Elovich, film and intraparticle diffusion models were used to analyze the kinetic data. Results showed that the pseudo-second order model can well describe the adsorption kinetic data. The thermodynamic parameters, such as Gibb's free energy change (ΔG°), standard enthalpy change (ΔH°) and standard entropy change (ΔS°) were also evaluated. Negative value of free energy at temperature range of 20–55 °C, indicates the spontaneous nature of Hg(II) sorption by ZnCl2-MCM-41 sorbent. The adsorption capacity which was found to decrease with temperature showed the exothermic nature of the mercury sorption process (ΔH° = −49.4 kJ mol−1). The negative ΔS° value (−148.9 J mol−1 K−1) revealed a decrease in the randomness at the solid/solution interface and also indicated the fast adsorption of the Hg(II) onto active sites

  13. Mercury's Messenger

    Science.gov (United States)

    Chapman, Clark R.

    2004-01-01

    Forty years after Mariner 2, planetary exploration has still only just begun, and many more missions are on drawing boards, nearing the launch pad, or even en route across interplanetary space to their targets. One of the most challenging missions that will be conducted this decade is sending the MESSENGER spacecraft to orbit the planet Mercury.…

  14. Uptake of mercury by thiol-grafted chitosan gel beads.

    Science.gov (United States)

    Merrifield, John D; Davids, William G; MacRae, Jean D; Amirbahman, Aria

    2004-07-01

    This study describes the synthesis and characterization of thiol-grafted chitosan beads for use as mercury (Hg) adsorbents. Chitosan flakes were dissolved and formed into spherical beads using a phase inversion technique, then crosslinked to improve their porosity and chemical stability. Cysteine was grafted onto the beads in order to improve the adsorption affinity of Hg to the beads. The beads possessed an average diameter of 3.2 mm, porosity of 0.9, specific surface area of approximately 100 m2/g, average pore size of approximately 120 angstroms, and specific gravity of 2.0. Equilibrium and kinetic uptake experiments were conducted to study the uptake of Hg by the beads. The adsorption capacity was approximately 8.0 mmol-Hg/g-dry beads at pH 7, and decreased with decreasing pH. Hg adsorption kinetics was modeled as radial pore diffusion into a spherical bead with nonlinear adsorption. Use of the nonlinear Freundlich isotherm in the diffusion equation allowed modeling of the uptake kinetics with a single tortuosity factor of 1.5 +/- 0.3 as the fitting parameter for all initial Hg concentrations, chitosan loadings, and agitation rates. At agitation rates of 50 and 75 rpm, where uptake rate was reduced significantly due to the boundary layer effect, the mass transfer coefficient at the outside boundary was also used as a fitting parameter to model the kinetic data. At agitation rates higher than 150 rpm, pore diffusion was the rate-limiting step. The beads exhibited a high initial uptake rate followed by a slower uptake rate suggesting pore diffusion as the rate-determining step especially at high agitation rates. Higher uptake rates observed in this study compared to those in a previous study of chitosan-based crab shells indicate that dissolution and gel formation increase the porosity and pore accessibility of chitosan.

  15. RECOVERY OF MERCURY FROM CONTAMINATED LIQUID WASTES

    Energy Technology Data Exchange (ETDEWEB)

    Robin M. Stewart

    1999-09-29

    magnetic field was evaluated. Field results indicated good removal of this mercury fraction from the Y-12 waters. In addition, this sorbent is easily regenerated by simply removing the magnetic field and flushing the columns with water. The fourth sorbent is still undergoing laboratory development, but results to date indicate exceptionally high mercury sorption capacity. The sorbent is capable of removing all forms of mercury typically present in natural and industrial waters, including Hg{sup 2+}, elemental mercury, methyl mercury, and colloidal mercury. The process possesses very fast kinetics, which allows for higher flow rates and smaller treatment units. These sorbent technologies, used in tandem or individually depending on the treatment needs, can provide DOE sites with a cost-effective method for reducing mercury concentrations to very low levels mandated by the regulatory community. In addition, the technologies do not generate significant amounts of secondary wastes for disposal. Furthermore, the need for improved water treatment technologies is not unique to the DOE. The new, stringent requirements on mercury concentrations impact other government agencies as well as the private sector. Some of the private-sector industries needing improved methods for removing mercury from water include mining, chloralkali production, chemical processing, and medical waste treatment. The next logical step is to deploy one or more of these sorbents at a contaminated DOE site or at a commercial facility needing improved mercury treatment technologies. A full-scale deployment is planned in fiscal year 2000.

  16. Evaluation of the capacity of heavy metal adsorption in exfoliated vermiculite; Avaliacao da capacidade de adsorcao de metal pesado em vermiculitas esfoliadas

    Energy Technology Data Exchange (ETDEWEB)

    Lima, J.F.; Silva, P.S.; Hanken, R.B.L. [Universidade Federal de Campina Grande (UAEMa/UFCG), PB (Brazil). Unidade Academica de Engenharia de Materiais; Raposo, C.M.O., E-mail: raposo@dmg.ufcg.edu.b [Universidade Federal de Campina Grande (UAMG/UFCG), Bodocongo, PB (Brazil). Unidade Academica de Mineracao e Geologia

    2009-07-01

    Many groups from modern society have seen with attention the issues of pollutants, generally present in nature, those same that have caused irreversible damages to the environment. The Vermiculite, a phyllosilicate, with t-o-t structure, have high interlamelar charge, has been studied as cationic exchanger, whose application when exfoliated, are increased. This work has the objective of evaluate the absorption capacity of chromium (III), in different concentrations, in high, slim and medium concentrations of exfoliated vermiculites. The results obtained from the characterization by spectroscopy in infrared and by diffraction of x-ray from prepared solids showed important variations in the quantity of adsorbed metal in order the size of the concentrated particles. (author)

  17. Phragmites karka as a Biosorbent for the Removal of Mercury Metal Ions from Aqueous Solution: Effect of Modification

    Directory of Open Access Journals (Sweden)

    Muhammad Hamid Raza

    2015-01-01

    Full Text Available Batch scale studies for the adsorption potential of novel biosorbent Phragmites karka (Trin, in its natural and treated forms, were performed for removal of mercury ions from aqueous solution. The study was carried out at different parameters to obtain optimum conditions of pH, biosorbent dose, agitation speed, time of contact, temperature, and initial metal ion concentration. To analyze the suitability of the process and maximum amount of metal uptake, Dubinin-Radushkevich (D-R model, Freundlich isotherm, and Langmuir isotherm were applied. The values of qmax for natural and treated biosorbents were found at 1.79 and 2.27 mg/g, respectively. The optimum values of contact time and agitation speed were found at 50 min and 150 rpm for natural biosorbent whereas 40 min and 100 rpm for treated biosorbent, respectively. The optimum biosorption capacities were observed at pH 4 and temperature 313 K for both natural P. karka and treated P. karka. RL values indicate that comparatively treated P. karka was more feasible for mercury adsorption compared to natural P. karka. Both pseudo-first-order and pseudo-second-order kinetic models were applied and it was found that data fit best to the pseudo-second-order kinetic model. Thermodynamic studies indicate that adsorption process was spontaneous, feasible, and endothermic.

  18. Biosorption of mercury from aqueous solutions using highly characterised peats

    Directory of Open Access Journals (Sweden)

    A.M. Rizzuti

    2015-02-01

    Full Text Available This research investigated the biosorption of mercury from aqueous solutions by six highly characterised peats. Samples of the peats were tested both in unaltered condition and after being treated with hydrochloric acid (HCl to free up any occupied exchange sites. Other variables tested were sample dose, contact time, mixing temperature, and the concentration and pH of the mercury solution. Desorption studies were also performed, and tests were done to determine whether the peats could be re-used for mercury biosorption. The results indicate that all six peat types biosorb mercury from aqueous solutions extremely well (92−100 % removal and that their mercury removal capacities are not significantly affected by manipulation of the various factors tested. The factor that had the greatest impact on the mercury removal capacities of the peats was the pH of the mercury solution. The optimal mercury solution pH for mercury removal was in the range 5−7 for four of the peats and in the range 2−3 for the other two. The desorption results indicate that it may be possible to recover up to 41 % of the removed mercury. All of the peat types tested can be repeatedly re-used for additional mercury biosorption cycles. Hence, their disposal should not become a hazardous waste problem.

  19. Removal of elemental mercury by iodine-modified rice husk ash sorbents

    Institute of Scientific and Technical Information of China (English)

    Pengfei Zhao; Xin Guo; Chuguang Zheng

    2010-01-01

    Iodine-modified calcium-based rice husk ash sorbents (I2/CaO/RHA) were synthesized and characterized by X-ray diffraction,X-ray fluorescence,and N2 isotherm adsorpdon/desorption.Adsorption experiments of vapor-phase elemental mercury (Hg0) were performed in a laboratory-scale fixed-bed reactor.I2/CaO/RHA performances on Hg0 adsorption were compared with those of modified Cabased fly ash sorbents (I2/CaO/FA) and modified fly ash sorbents (I2/FA).Effects of oxidant loading,supports,pore size distribution,iodine impregnation modes,and temperature were investigated as well to understand the mechanism in capturing Hg0.The modified sorbents exhibited reasonable efficiency for Hg0 removal under simulated flue gas.The surface area,pore size distribution,and iodine impregnation modes of the sorbents did not produce a strong effect on Hg0 capture efficiency,while fair correlation was observed between Hg0 uptake capacity and iodine concentration.Therefore,the content of I2 impregnated on the sorbents was identified as the most important factor influencing the capacity of these sorbents for Hg0 uptake.Increasing temperature in the range of 80-140℃ caused a rise in Hg0 removal.A reaction mechanism that may explain the experimental results was presumed based on the characterizations and adsorption study.

  20. 改性褐煤活性焦对模拟烟气中汞的脱除研究%Influence of modified lignite activated coke on mercury removal from simulated flue gas

    Institute of Scientific and Technical Information of China (English)

    吴鹏; 滕济林; 张旭辉; 赵悦菊

    2015-01-01

    为降低烟气脱汞成本,提高活性焦脱汞性能,以内蒙古锡林浩特褐煤为原料制备活性焦并进行化学改性,分析载硫、Na2 S溶液和ZnCl2溶液浸渍等改性方法对活性焦结构及性能的影响,研究改性方法、吸附温度、负载量和汞渗透量对活性焦脱汞性能的影响。结果表明,活性焦改性后,比表面积和孔容积有所降低,载Na2 S、硫、ZnCl2活性焦对汞的吸附量比原始活性焦分别提高了60%、113%和140%;吸附温度升高,化学反应变快,活性焦的初始脱汞效率由75.8%提高至95%以上,但穿透时间并不呈比例增加;当ZnCl2负载量由5%提高至15%后,50%穿透率对应时间由75 min延长至120 min,活性焦对汞的吸附值由10.1μg/g增至17.5μg/g。随着汞渗透量的增加,活性焦脱汞效率有所提高,50%穿透率的对应时间由110 min缩短至95 min,最终总吸附值仅由14.4μg/g增至16.2μg/g。%In order to reduce mercury removal cost from flue gas and improve mercury removal performance of activated coke,the Xilinhot lignite was chosen to prepare activated coke which was further modified by a series of chemical methods. The influence of sulfur,Na2 S, ZnCl2 impregnating on the structure and properties of activated coke was studied. Further more,the effects of modified methods,adsorbent temperature,capacity and mercury infiltration capacity on activated coke mercury removal performance were researched. The results showed that,after modification,the specific surface area and pore volume of activated coke decreased. Compared to the original activated coke,mer-cury adsorption of AC-Na2 S,AC-S and AC-ZnCl2 was respectively increased by 60%,113% and 140%. With the proportion of modifier to activated coke increased,the mercury adsorption capacity increased. With the adsorption temperature increased,the chemical reaction became faster,the initial efficiency of mercury removal could be increased from 75. 8% to

  1. Assessing sorbent injection mercury control effectiveness in flue gas streams

    Science.gov (United States)

    Carey, T.R.; Richardson, C.F.; Chang, R.; Meserole, F.B.; Rostam-Abadi, M.; Chen, S.

    2000-01-01

    One promising approach for removing mercury from coal-fired, utility flue gas involves the direct injection of mercury sorbents. Although this method has been effective at removing mercury in municipal waste incinerators, tests conducted to date on utility coal-fired boilers show that mercury removal is much more difficult in utility flue gas. EPRI is conducting research to investigate mercury removal using sorbents in this application. Bench-scale, pilot-scale, and field tests have been conducted to determine the ability of different sorbents to remove mercury in simulated and actual flue gas streams. This paper focuses on recent bench-scale and field test results evaluating the adsorption characteristics of activated carbon and fly ash and the use of these results to develop a predictive mercury removal model. Field tests with activated carbon show that adsorption characteristics measured in the lab agree reasonably well with characteristics measured in the field. However, more laboratory and field data will be needed to identify other gas phase components which may impact performance. This will allow laboratory tests to better simulate field conditions and provide improved estimates of sorbent performance for specific sites. In addition to activated carbon results, bench-scale and modeling results using fly ash are presented which suggest that certain fly ashes are capable of adsorbing mercury.

  2. Recovery of Mercury From Contaminated Liquid Wastes

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1998-06-12

    The Base Contract program emphasized the manufacture and testing of superior sorbents for mercury removal, testing of the sorption process at a DOE site, and determination of the regeneration conditions in the laboratory. During this project, ADA Technologies, Inc. demonstrated the following key elements of a successful regenerable mercury sorption process: (1) sorbents that have a high capacity for dissolved, ionic mercury; (2) removal of ionic mercury at greater than 99% efficiency; and (3) thermal regeneration of the spent sorbent. ADA's process is based on the highly efficient and selective sorption of mercury by noble metals. Contaminated liquid flows through two packed columns that contain microporous sorbent particles on which a noble metal has been finely dispersed. A third column is held in reserve. When the sorbent is loaded with mercury to the point of breakthrough at the outlet of the second column, the first column is taken off-line and the flow of contaminated liquid is switched to the second and third columns. The spent column is regenerated by heating. A small flow of purge gas carries the desorbed mercury to a capture unit where the liquid mercury is recovered. Laboratory-scale tests with mercuric chloride solutions demonstrated the sorbents' ability to remove mercury from contaminated wastewater. Isotherms on surrogate wastes from DOE's Y-12 Plant in Oak Ridge, Tennessee showed greater than 99.9% mercury removal. Laboratory- and pilot-scale tests on actual Y-12 Plant wastes were also successful. Mercury concentrations were reduced to less than 1 ppt from a starting concentration of 1,000 ppt. The treatment objective was 50 ppt. The sorption unit showed 10 ppt discharge after six months. Laboratory-scale tests demonstrated the feasibility of sorbent regeneration. Results show that sorption behavior is not affected after four cycles.

  3. Recovery of Mercury From Contaminated Liquid Wastes

    International Nuclear Information System (INIS)

    The Base Contract program emphasized the manufacture and testing of superior sorbents for mercury removal, testing of the sorption process at a DOE site, and determination of the regeneration conditions in the laboratory. During this project, ADA Technologies, Inc. demonstrated the following key elements of a successful regenerable mercury sorption process: (1) sorbents that have a high capacity for dissolved, ionic mercury; (2) removal of ionic mercury at greater than 99% efficiency; and (3) thermal regeneration of the spent sorbent. ADA's process is based on the highly efficient and selective sorption of mercury by noble metals. Contaminated liquid flows through two packed columns that contain microporous sorbent particles on which a noble metal has been finely dispersed. A third column is held in reserve. When the sorbent is loaded with mercury to the point of breakthrough at the outlet of the second column, the first column is taken off-line and the flow of contaminated liquid is switched to the second and third columns. The spent column is regenerated by heating. A small flow of purge gas carries the desorbed mercury to a capture unit where the liquid mercury is recovered. Laboratory-scale tests with mercuric chloride solutions demonstrated the sorbents' ability to remove mercury from contaminated wastewater. Isotherms on surrogate wastes from DOE's Y-12 Plant in Oak Ridge, Tennessee showed greater than 99.9% mercury removal. Laboratory- and pilot-scale tests on actual Y-12 Plant wastes were also successful. Mercury concentrations were reduced to less than 1 ppt from a starting concentration of 1,000 ppt. The treatment objective was 50 ppt. The sorption unit showed 10 ppt discharge after six months. Laboratory-scale tests demonstrated the feasibility of sorbent regeneration. Results show that sorption behavior is not affected after four cycles

  4. 改性橘子皮对水中金属离子的吸附%The Adsorptive Capacity of Zinc and Iron of Water by Modified Orange Peel

    Institute of Scientific and Technical Information of China (English)

    毛娜

    2014-01-01

    将橘子皮用氢氧化钾、乙醇和氯化钙进行皂化处理,得到改性橘子皮生物吸附剂( SCOP)。在保持pH、起始金属离子浓度和温度不变的情况下进行吸附试验,研究不同氢氧化钾浓度浸泡下的SCOP及不同固液比、接触时间的改性橘子皮对水中锌、铁离子的吸附量大小。通过火焰原子吸收分光光度计定性测得SCOP对锌离子有较好的吸附,对铁则吸附较少。%A novel absorbent was prepared by modifying orange peel with potassium hydroxide and calcium chloride. Keeping pH, initial concentration of metal ions and experimental temperature not change, the absorption behavior of Zn( II) and Fe ( II ) on modified orange peel under varying concentration of sodium hydroxide, contract time and absorption of different quantity were studied. SCOP had a better adsorption capacities for Zn ( II ) but with a fewer for Fe( II) by flame atomic absorption spectrometry.

  5. Mercury emission, control and measurement from coal combustion

    Energy Technology Data Exchange (ETDEWEB)

    Pan, Wei-Ping [North China Electric Power Univ., Beijing (China). School of Energy and Power Engineering; Western Kentucky Univ., Bowling Green, KY (United States). Inst. for Combustion Science and Environmental Technology; Cao, Yan [Western Kentucky Univ., Bowling Green, KY (United States). Inst. for Combustion Science and Environmental Technology; Zhang, Kai [North China Electric Power Univ., Beijing (China). School of Energy and Power Engineering

    2013-07-01

    that are only equipped with an Electrostatic Precipitator (ESP) have to look for a control method to reduce mercury emission. So far, the most economical method has been active carbon or sorbent injection before the ESP. Active carbon or sorbent injected into the flue gas ducts to oxidize the elemental mercury and then the oxidized mercury will be captured from the flue gas, then the ESP captures the active carbon or sorbent and fly ash simultaneously. Therefore, the long distance transportation of gaseous mercury is eliminated. However, the capture efficiency of mercury is extremely important in order to reduce the increase in ESP load and control the cost. The oxidation and adsorption rate of HBr and fly ash will be discussed in this presentation.

  6. Mercury Control with Calcium-Based Sorbents and Oxidizing Agents

    Energy Technology Data Exchange (ETDEWEB)

    Thomas K. Gale

    2005-07-01

    This Final Report contains the test descriptions, results, analysis, correlations, theoretical descriptions, and model derivations produced from many different investigations performed on a project funded by the U.S. Department of Energy, to investigate calcium-based sorbents and injection of oxidizing agents for the removal of mercury. Among the technologies were (a) calcium-based sorbents in general, (b) oxidant-additive sorbents developed originally at the EPA, and (c) optimized calcium/carbon synergism for mercury-removal enhancement. In addition, (d) sodium-tetrasulfide injection was found to effectively capture both forms of mercury across baghouses and ESPs, and has since been demonstrated at a slipstream treating PRB coal. It has been shown that sodium-tetrasulfide had little impact on the foam index of PRB flyash, which may indicate that sodium-tetrasulfide injection could be used at power plants without affecting flyash sales. Another technology, (e) coal blending, was shown to be an effective means of increasing mercury removal, by optimizing the concentration of calcium and carbon in the flyash. In addition to the investigation and validation of multiple mercury-control technologies (a through e above), important fundamental mechanism governing mercury kinetics in flue gas were elucidated. For example, it was shown, for the range of chlorine and unburned-carbon (UBC) concentrations in coal-fired utilities, that chlorine has much less effect on mercury oxidation and removal than UBC in the flyash. Unburned carbon enhances mercury oxidation in the flue gas by reacting with HCl to form chlorinated-carbon sites, which then react with elemental mercury to form mercuric chloride, which subsequently desorbs back into the flue gas. Calcium was found to enhance mercury removal by stabilizing the oxidized mercury formed on carbon surfaces. Finally, a model was developed to describe these mercury adsorption, desorption, oxidation, and removal mechanisms, including

  7. Mercury contamination extraction

    Science.gov (United States)

    Fuhrmann, Mark; Heiser, John; Kalb, Paul

    2009-09-15

    Mercury is removed from contaminated waste by firstly applying a sulfur reagent to the waste. Mercury in the waste is then permitted to migrate to the reagent and is stabilized in a mercury sulfide compound. The stable compound may then be removed from the waste which itself remains in situ following mercury removal therefrom.

  8. Phosphate adsorption on lanthanum loaded biochar.

    Science.gov (United States)

    Wang, Zhanghong; Shen, Dekui; Shen, Fei; Li, Tianyu

    2016-05-01

    To attain a low-cost and high-efficient phosphate adsorbent, lanthanum (La) loaded biochar (La-BC) prepared by a chemical precipitation method was developed. La-BC and its pristine biochar (CK-BC) were comparatively characterized using zeta potential, BET surface area, scanning electron microscopy/energy dispersive spectrometer (SEM-EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FT-IR). The adsorption ability and the mechanisms during adsorption process for the La-BC samples were also investigated. La loaded on the surface of biochar can be termed as La-composites (such as LaOOH, LaONO3 and La(OH)3), leading to the decrease of negative charge and surface area of biochar. La-BC exhibited the high adsorption capacity to phosphate compared to CK-BC. Adsorption isotherm and adsorption kinetic studies showed that the Langmuir isotherm and second order model could well describe the adsorption process of La-BC, indicating that the adsorption was dominated by a homogeneous and chemical process. The calculated maximum adsorption capacity was as high as 46.37 mg g(-1) (computed in P). Thermodynamic analysis revealed that the adsorption was spontaneous and endothermic. SEM, XRD, XPS and FT-IR analysis suggested that the multi-adsorption mechanisms including precipitation, ligand exchange and complexation interactions can be evidenced during the phosphate adsorption process by La-composites in La-BC. PMID:26871732

  9. Mercury and health care

    Directory of Open Access Journals (Sweden)

    Rustagi Neeti

    2010-01-01

    Full Text Available Mercury is toxic heavy metal. It has many characteristic features. Health care organizations have used mercury in many forms since time immemorial. The main uses of mercury are in dental amalgam, sphygmomanometers, and thermometers. The mercury once released into the environment can remain for a longer period. Both acute and chronic poisoning can be caused by it. Half of the mercury found in the atmosphere is human generated and health care contributes the substantial part to it. The world has awakened to the harmful effects of mercury. The World Health Organization and United Nations Environmental Programme (UNEP have issued guidelines for the countries′ health care sector to become mercury free. UNEP has formed mercury partnerships between governments and other stakeholders as one approach to reducing risks to human health and the environment from the release of mercury and its compounds to the environment. Many hospitals are mercury free now.

  10. Mercury and health care

    Science.gov (United States)

    Rustagi, Neeti; Singh, Ritesh

    2010-01-01

    Mercury is toxic heavy metal. It has many characteristic features. Health care organizations have used mercury in many forms since time immemorial. The main uses of mercury are in dental amalgam, sphygmomanometers, and thermometers. The mercury once released into the environment can remain for a longer period. Both acute and chronic poisoning can be caused by it. Half of the mercury found in the atmosphere is human generated and health care contributes the substantial part to it. The world has awakened to the harmful effects of mercury. The World Health Organization and United Nations Environmental Programme (UNEP) have issued guidelines for the countries’ health care sector to become mercury free. UNEP has formed mercury partnerships between governments and other stakeholders as one approach to reducing risks to human health and the environment from the release of mercury and its compounds to the environment. Many hospitals are mercury free now. PMID:21120080

  11. Mercury and health care.

    Science.gov (United States)

    Rustagi, Neeti; Singh, Ritesh

    2010-08-01

    Mercury is toxic heavy metal. It has many characteristic features. Health care organizations have used mercury in many forms since time immemorial. The main uses of mercury are in dental amalgam, sphygmomanometers, and thermometers. The mercury once released into the environment can remain for a longer period. Both acute and chronic poisoning can be caused by it. Half of the mercury found in the atmosphere is human generated and health care contributes the substantial part to it. The world has awakened to the harmful effects of mercury. The World Health Organization and United Nations Environmental Programme (UNEP) have issued guidelines for the countries' health care sector to become mercury free. UNEP has formed mercury partnerships between governments and other stakeholders as one approach to reducing risks to human health and the environment from the release of mercury and its compounds to the environment. Many hospitals are mercury free now.

  12. Surface Modification, Surface Groups Characterization and Adsorption Properties of Bamboo-Charcoal%竹炭的表面改性、基团表征与吸附性能

    Institute of Scientific and Technical Information of China (English)

    张启伟; 王桂仙

    2012-01-01

    Surface of ordinary bamboo-charcoal was pretreated with nitric acid and microwave heating,ammonia. Fourier transform infrared( FTIR) spectrometer, elemental analysis measurements demonstrate that the contents of O-containing groups and N-containing groups on the bamboo-charcoal surface increase via HNO3 and NH3 · H20 treatment. Results showed of adsorption that adsorption capacity of the modified bamboo-charcoal for metal ions were elevated remarkably. Among them, the mercury(Ⅱ) adsorption capacity increased by 25% , and palladium(Ⅱ) adsorption capacity increased by 32% or more. And the adsorption process was changed from the physical adsorption to the chemical adsorption. This study will expanded the applications of bamboo charcoal, and become into functional adsorption material.%通过硝酸+微波加热和氨水吸附的方法对普通竹炭进行表面改性处理,运用红外图谱和元素分析对改性前后的竹炭进行表征.结果表明:含氧基团和含氮基团的含量明显增加.吸附试验结果表明:改性后竹炭对金属离子的吸附性能明显提高,其中,汞(Ⅱ)的吸附量提高25%以上,钯(Ⅱ)的吸附量提高32%以上,且吸附过程从以物理吸附为主转化为以化学吸附为主.

  13. Mercury and health care

    OpenAIRE

    Rustagi Neeti; Singh Ritesh

    2010-01-01

    Mercury is toxic heavy metal. It has many characteristic features. Health care organizations have used mercury in many forms since time immemorial. The main uses of mercury are in dental amalgam, sphygmomanometers, and thermometers. The mercury once released into the environment can remain for a longer period. Both acute and chronic poisoning can be caused by it. Half of the mercury found in the atmosphere is human generated and health care contributes the substantial part to it. The world ha...

  14. Selective adsorption of tannins onto hide collagen fibres

    Institute of Scientific and Technical Information of China (English)

    LIAO; Xuepin(廖学品); LU; Zhongbing(陆忠兵); SHI; Bi(石碧)

    2003-01-01

    Hide collagen of animals is used to prepare adsorbent material and its adsorption properties to tannins are investigated. It is indicated that the collagen fibres has excellent adsorption selectivity and high adsorption capacity to tannins. The adsorption rate of tannins is more than 90% whilst less than 10% of functional components are retained by the adsorbent. The adsorption mechanism of tannins onto hide collagen fibres is hydrogen-bonding association. Freundlich model can be used to describe the adsorption isotherms, and the pseudo-second-order rate model can be used to describe adsorption kinetics.

  15. Voltammetric and theoretical studies of electrochemical behavior of cephalosporins at the mercury electrode

    Directory of Open Access Journals (Sweden)

    Nikolić Katarina

    2015-01-01

    Full Text Available Study of the adsorption and electroreduction behavior of cefpodoxime proxetil, cefotaxime, desacetylcefotaxime, cefetamet, ceftriaxone, ceftazidime, and cefuroxime axetile at the mercury electrode surface has been performed using Cyclic (CV, Differential Pulse (DPV, and Adsorptive Stripping Differential Pulse Voltammetry (AdSDPV. The Quantitative Structure Property Relationship (QSPR study of the seven cephalosporins adsorption at the mercury electrode has been based on the density functional theory DFT-B3LYP/6-31G (d,p calculations of molecular orbitals, partial charges and electron densities of analytes. The DFT-parameters and QSPR model explain well the process of adsorption of the examined cephalosporins. QSPR study defined that cefalosporins with lower charge of sulphur in the thiazine moiety, lower electron density on the nitrogen atom of the N-O bond, higher number of hydrogen bond accepting groups, and higher principal moment of inertia should express high adsorption on the mercury electrode. [Projekat Ministarstva nauke Republike Srbije, br. 172033

  16. Impacts of acid gases on mercury oxidation across SCR catalyst

    International Nuclear Information System (INIS)

    A series of bench-scale experiments were completed to evaluate acid gases of HCl, SO2, and SO3 on mercury oxidation across a commercial selective catalytic reduction (SCR) catalyst. The SCR catalyst was placed in a simulated flue gas stream containing O2, CO2, H2O, NO, NO2, and NH3, and N2. HCl, SO2, and SO3 were added to the gas stream either separately or in combination to investigate their interactions with mercury over the SCR catalyst. The compositions of the simulated flue gas represent a medium-sulfur and low- to medium-chlorine coal that could represent either bituminous or subbituminous. The experimental data indicated that 5-50 ppm HCl in flue gas enhanced mercury oxidation within the SCR catalyst, possibly because of the reactive chlorine species formed through catalytic reactions. An addition of 5 ppm HCl in the simulated flue gas resulted in mercury oxidation of 45% across the SCR compared to only 4% mercury oxidation when 1 ppm HCl is in the flue gas. As HCl concentration increased to 50 ppm, 63% of Hg oxidation was reached. SO2 and SO3 showed a mitigating effect on mercury chlorination to some degree, depending on the concentrations of SO2 and SO3, by competing against HCl for SCR adsorption sites. High levels of acid gases of HCl (50 ppm), SO2 (2000 ppm), and SO3 (50 ppm) in the flue gas deteriorate mercury adsorption on the SCR catalyst. (author)

  17. Mercury Quick Facts: Health Effects of Mercury Exposure

    Science.gov (United States)

    Mercury Quick Facts Health Effects of Mercury Exposure What is Elemental Mercury? Elemental (metallic) mercury is the shiny, silver-gray metal found in thermometers, barometers, and thermostats and other ...

  18. Characterization for Adsorption of Vapor-phase HgCl2 on Coconut Shell Activated Carbon%椰壳活性炭对气态氯化汞吸附作用的对比研究

    Institute of Scientific and Technical Information of China (English)

    孙康; 何跃; 卢辛成; 蒋剑春; 陈水根

    2015-01-01

    以氯化汞为目标污染物,研究了椰壳活性炭对气态氯化汞的吸附性能,并结合活性炭微结构表征以及动力学模型拟合研究了其吸附机理。结果表明,椰壳活性炭对气态氯化汞的最大吸附量35.9 mg/g,且活性炭比表面积和总孔容对其吸附氯化汞有显著影响,比表面积大、总孔容大有利于提高饱和吸附量。载气流量不影响活性炭对氯化汞的饱和吸附量,但是影响其吸附时间,增大载气流量能够缩短吸附时间。温度对吸附量和吸附时间均有影响,升高温度能够提高吸附量且缩短吸附时间。通过对吸附过程的动力学模拟,发现活性炭对氯化汞的吸附均符合班厄姆动力学模型,相关系数均大于0.99,活性炭的吸附速率与吸附量随比表面积与总孔容的增大而增大。%With mercury chloride as pollution target, the adsorption properties of activated carbons for vapor-phase HgCl2 were investigated. Combining with structural characterization and dynamic model fitting,the adsorption mechanism was discussed. The results indicated that the adsorption capacity of HgCl2 on coco-nut shell activated carbon was 35. 9 mg/g and obviously influenced by surface area and total volume. The gas flow didn ’ t influence the saturated adsorption quantity but the adsorption time is affected. The increase of the gas flow could shorten the adsorption time. The temperature affected the adsorption capacity and adsorption time,and raising temperature could increase the adsorption capacity and shorten the adsorption time. From the kinetic study,it was found that the HgCl2 adsorption process of the activated carbon could be described by Bangham model with R2 >0. 99,and the adsorption rate and capacity increased with the increase of surface area and total volume.

  19. [Adsorption and Desorption Characteristics of Endosulfan in Purple Soil].

    Science.gov (United States)

    Zhao, Yan; Zheng, Guo-can; Zhu, Heng; Zhang, Jin-zhong; Zhu, Xiu-ying; Hu, Shu-chun; Wu, Ya-lin

    2015-09-01

    In order to reveal the residual process of endosulfan in purple soil and protect soil ecological environment, the adsorption and desorption characteristics of endosulfan in purple soil were investigated, and effects of temperature, adsorbent amount, and initial pH of adsorption solution on the adsorption capacity were also examined by static adsorption and desorption experiments. The results showed that the adsorption kinetic process could be well described by the second-order kinetic equation with the initial rate constants of α-, β-endosulfan as 0. 157 and 0. 115 mg.(g.min)-1, respectively. The adsorption thermodynamic process could be well described by the Langmuir isotherm with the maximum adsorption capacities of α-, β-endosulfan as 0. 257 mg . g -1 and 0. 155 mg . g -1, respectively. The adsorption process of endosulfan in purple soil may be an exothermic physicochemical process, and is dominated by physical adsorption. Under the experimental conditions examined in this study, the initial pH of adsorption solution had a relative great influence on the adsorption capacity, whereas the temperature and adsorbent amount had no significant influence. The desorption experiments found that the maximum desorption capacities of α-, β-endosulfan adsorbed in purple soil were 0. 029 mg . g -1 and 0. 017 mg . g -1 at 6 and 4 h, and accounted for 10. 5% and 16. 1% in the maximum adsorption capacities, respectively. PMID:26717711

  20. Macroalgae response to a mercury contamination gradient in a temperate coastal lagoon (Ria de Aveiro, Portugal)

    OpenAIRE

    Coelho, J.P.; Pereira, M. E.; Duarte, A.; Pardal, M.A.

    2005-01-01

    Primary producers represent an important pathway for mercury incorporation in aquatic food webs. With eutrophication processes occurring worldwide, macroalgae may represent a substantial pool of mercury, as a result of its high growth rate and capacity to bind trace metals. The main aim of this work was to evaluate the response of the macroalgae to a human-induced environmental mercury gradient in a temperate coastal lagoon, by assessing the total and organic mercury contamination levels of t...

  1. Adsorption of amitraz on the clay

    Directory of Open Access Journals (Sweden)

    Jale Gülen

    2013-01-01

    Full Text Available Amitraz (AZ that is used as acaridies was tried to extract with a clay. The experimental data were modelled as using Langmuir and Freundlich isotherms. The adsorption data fit well with Langmuir isotherm that indicated the AZ adsorption is homogeneous and monolayer. The monolayer adsorption capacity was found to be 35.02 mg/g at 20 ºC temperature. Effect of the phases contact time, the initial solution pH and the initial pesticide concentration were investigated from the point of adsorption equilibrium and yield. The adsorption kinetics were investigated by applying pseudo first order, pseudo second order and intra particle diffusion laws. Adsorption of AZ was found to be best fitted by the pseudo second order model. The intra particle diffusion also plays an important role in adsorption phenomenon.

  2. Aerobic Mercury-resistant bacteria alter Mercury speciation and retention in the Tagus Estuary (Portugal).

    Science.gov (United States)

    Figueiredo, Neusa L; Canário, João; O'Driscoll, Nelson J; Duarte, Aida; Carvalho, Cristina

    2016-02-01

    Aerobic mercury-resistant bacteria were isolated from the sediments of two highly mercury-polluted areas of the Tagus Estuary (Barreiro and Cala do Norte) and one natural reserve area (Alcochete) in order to test their capacity to transform mercury. Bacterial species were identified using 16S rRNA amplification and sequencing techniques and the results indicate the prevalence of Bacillus sp. Resistance patterns to mercurial compounds were established by the determination of minimal inhibitory concentrations. Representative Hg-resistant bacteria were further tested for transformation pathways (reduction, volatilization and methylation) in cultures containing mercury chloride. Bacterial Hg-methylation was carried out by Vibrio fluvialis, Bacillus megaterium and Serratia marcescens that transformed 2-8% of total mercury into methylmercury in 48h. In addition, most of the HgR bacterial isolates showed Hg(2+)-reduction andHg(0)-volatilization resulting 6-50% mercury loss from the culture media. In summary, the results obtained under controlled laboratory conditions indicate that aerobic Hg-resistant bacteria from the Tagus Estuary significantly affect both the methylation and reduction of mercury and may have a dual face by providing a pathway for pollution dispersion while forming methylmercury, which is highly toxic for living organisms.

  3. Mercury transformation and speciation in flue gases from anthropogenic emission sources: a critical review

    Directory of Open Access Journals (Sweden)

    L. Zhang

    2015-11-01

    Full Text Available Mercury transformation mechanisms and speciation profiles are reviewed for mercury formed in and released from flue gases of coal-fired boilers, non-ferrous metal smelters, cement plants, iron and steel plants, municipal solid waste incinerators, and biomass burning. Mercury in coal, ores and other raw materials is released to flue gases in the form of Hg0 during combustion or smelting in boilers, kilns or furnaces. Decreasing temperature from over 800 °C to below 300 °C in flue gases leaving boilers, kilns or furnaces promotes homogeneous and heterogeneous oxidation of gaseous elemental mercury (Hg0 to gaseous divalent mercury (Hg2+, with a portion of Hg2+ adsorbed onto fly ash to form particulate-bound mercury (Hgp. Halogen is the primary oxidizer for Hg0 in flue gases, and active components (e.g.,TiO2, Fe2O3, etc. on fly ash promote heterogeneous oxidation and adsorption processes. In addition to mercury removal, mercury transformation also occurs when passing through air pollution control devices (APCDs, affecting the mercury speciation in flue gases. In coal-fired power plants, selective catalytic reduction (SCR system promotes mercury oxidation by 34–85 %, electrostatic precipitator (ESP and fabric filter (FF remove over 99 % of Hgp, and wet flue gas desulfurization system (WFGD captures 60–95 % of Hg2+. In non-ferrous metal smelters, most Hg0 is converted to Hg2+ and removed in acid plants (APs. For cement clinker production, mercury cycling and operational conditions promote heterogeneous mercury oxidation and adsorption. The mercury speciation profiles in flue gases emitted to the atmosphere are determined by transformation mechanisms and mercury removal efficiencies by various APCDs. For all the sectors reviewed in this study, Hgp accounts for less than 5 % in flue gases. In China, mercury emission has a higher fraction (66–82 % of total mercury in flue gases from coal combustion, in contrast to a greater Hg2+ fraction (29–90

  4. Enhanced sorption of mercury from compact fluorescent bulbs and contaminated water streams using functionalized multiwalled carbon nanotubes

    International Nuclear Information System (INIS)

    Highlights: • Oxidized (CNT-OX), CNT-I, CNT-S were prepared. • Capacity of CNT-S (151.5 mg/g) was higher than other CNTs. • Applied to the removal of Hg(II) from spiked and natural coal wash waters. • Applied to the removal of Hg(0) from compact fluorescent lamps. - Abstract: Three different functionalized multiwalled carbon nanotubes were prepared, namely, oxidized CNTs (CNT-OX), iodide incorporated MWCNT (CNT-I) and sulfur incorporated MWCNT (CNT-S). The as prepared adsorbents were structurally characterized by various spectral techniques like scanning electron microscopy (SEM), energy dispersive X-ray (EDAX), Brunauer, Emmett, and Teller (BET) surface area analyzer, Fourier transform infra red (FTIR) and Raman spectroscopy. Loading of iodide and sulfur was evident from the EDAX graphs. The adsorption properties of Hg2+ as a function of pH, contact time and initial metal concentration were characterized by Cold vapor AAS. The adsorption kinetics fitted the Pseudo second order kinetics and equilibrium was reached within 90 min. The experimental data were modeled with Langmuir, Freundlich, Dubinin-Redushkevich and Temkin isotherms and various isotherm parameters were evaluated. It was found that the mercury adsorption capacity for the prepared adsorbents were in the order of CNT-S > CNT-I > CNT-OX > CNT. Studies have been conducted to demonstrate the applicability of the sorbent toward the removal of Hg(0) from broken compact fluorescent light (CFL) bulbs and Hg(II) from contaminated water streams

  5. Adsorption of Atenolol on Kaolinite

    Directory of Open Access Journals (Sweden)

    Yingmo Hu

    2015-01-01

    Full Text Available In this study the adsorption of atenolol (AT, a β-blocker, on kaolinite, a clay mineral of low surface charge, was investigated under varying initial AT concentration, equilibrium time, solution pH, ionic strength, and temperature conditions. The results showed that the amounts of AT uptake by kaolinite were close to its cation exchange capacity value and the AT adsorption was almost instantaneous, suggesting a surface adsorption. The adsorption was exothermic and the free energy of adsorption was small negative, indicating physical adsorption. The increase in ionic strength of the solution drastically reduced AT uptake on kaolinite. A significant reduction in AT uptake was found at solution pH below 5 or above 10. The FTIR results showed band shifting and disappearance for NH bending vibration and benzene ring skeletal vibration at 3360 and 1515 cm−1 and band splitting at 1412 and 1240 cm−1 attributed to C–N valence vibration coupled with NH bending vibrations and alkyl aryl ether linkage, suggesting the participation of NH, –O–, and benzene ring for AT adsorption on kaolinite.

  6. Global trends in mercury management.

    Science.gov (United States)

    Kim, Dae-Seon; Choi, Kyunghee

    2012-11-01

    The United Nations Environmental Program Governing Council has regulated mercury as a global pollutant since 2001 and has been preparing the mercury convention, which will have a strongly binding force through Global Mercury Assessment, Global Mercury Partnership Activities, and establishment of the Open-Ended Working Group on Mercury. The European Union maintains an inclusive strategy on risks and contamination of mercury, and has executed the Mercury Export Ban Act since December in 2010. The US Environmental Protection Agency established the Mercury Action Plan (1998) and the Mercury Roadmap (2006) and has proposed systematic mercury management methods to reduce the health risks posed by mercury exposure. Japan, which experienced Minamata disease, aims vigorously at perfection in mercury management in several ways. In Korea, the Ministry of Environment established the Comprehensive Plan and Countermeasures for Mercury Management to prepare for the mercury convention and to reduce risks of mercury to protect public health. PMID:23230466

  7. Fator capacidade de fósforo em solos de pernambuco mineralogicamente diferentes e influência do pH na capacidade máxima de adsorção Phosphate capacity factor in mineralogically different soils in Pernambuco and the influence of pH on the maximum capacity of adsorption

    Directory of Open Access Journals (Sweden)

    Fábio Broggi

    2011-02-01

    -plant relations. Moreover, the soil pH has affected adsorption, and in other cases, it has shown small and inconsistent change in the maximum adsorption capacity of P (CMAP. Thus, this study aimed to determine the different FCP soil mineralogy in Pernambuco; to correlate physical and chemical characteristics of soils with PBC and to evaluate the effect of pH on the CMAP. Subsurface soil samples from four different soils were characterized chemically and physically determined, and the PBC was determined. These samples were corrected with CaCO3 and MgCO3 in a 4:1 ratio and incubated for 30 days, except the Vertisol. The CMAP was determined before and after correction of the soil. The experiment consisted of a 4 x 2 factorial (four soils with and without correction, distributed in randomized blocks with three replicates. Soil characteristics that best reflected the PBC were the remaining P (P-rem and MPAC. Regardless of the constituents of clay mineralogy, soil with high aluminum levels had increased CMAP after correction. The energy of adsorption (EA in the limed soils was on average significantly lower, regardless of the soil.

  8. 榴莲壳内皮果胶多糖和黄酮对重金属吸附作用的研究%Study on pectin polysaccharides and flavonoids extraction of durian inner shell on adsorption capacity of heavy metals

    Institute of Scientific and Technical Information of China (English)

    王晓波; 车海萍; 陈海珍; 刘冬英; 王梅

    2011-01-01

    目的:从榴莲壳内皮中提取果胶多糖和黄酮,并评价果胶多糖和黄酮对重金属的吸附作用。方法:以榴莲壳内皮为原料,采取水提乙醇沉淀法从榴莲壳内皮中提取高酯果胶及黄酮,采用碱化法将高酯果胶转化为低酯果胶,并用原子吸收光谱法测定高酯果胶、低酯果胶及黄酮对重金属的吸附率,从而评价其吸附能力。结果:在模拟胃液及肠液条件下,高酯果胶、低酯果胶和黄酮对铅的吸附能力:高酯果胶〉低酯果胶〉黄酮,对镉的吸附能力:低酯果胶〉高酯果胶〉黄酮;对钙、铁及锌离子均无吸附能力。结论:榴莲壳内皮中提取物果胶及黄酮对重金属元素有一定的选择性吸附作用,具有进一步研究和开发价值。%Objective:Study on pectin polysaccharides and flavonoids from durian inner shell and the adsorption capacity of the heavy metal. Methods:The durian inner shell as raw materials to ethanol precipitation,water extraction were directly extracted,high ester pectin and flavonoids,using alkaline method into the high-ester pectin with low ester pectin,to evaluate their adsorption capacity by atomic absorption spectrometry. Results:In simulated gastric and intestinal fluid conditions,the high ester pectin,low ester pectin and flavonoids adsorption capacity of Pb2+:high ester pectinlow ester pectinflavonoids,the adsorption capacity of Cd2+:low ester pectinhigh ester pectinflavonoids. There was no significant influence on Fe2+,Zn2+,Ca2+ absorption. Conclusion:The pectin and flavonoids extraction from durian inner shell had a certain heavy metal adsorption capacity,with research and development value.

  9. Nanosized cation-deficient Fe-Ti spinel: a novel magnetic sorbent for elemental mercury capture from flue gas.

    Science.gov (United States)

    Yang, Shijian; Guo, Yongfu; Yan, Naiqiang; Wu, Daqing; He, Hongping; Qu, Zan; Yang, Chen; Zhou, Qin; Jia, Jinping

    2011-02-01

    Nonstoichiometric Fe-Ti spinel (Fe(3-x)Ti(x))(1-δ)O(4) has a large amount of cation vacancies on the surface, which may provide active sites for pollutant adsorption. Meanwhile, its magnetic property makes it separable from the complex multiphase system for recycling, and for safe disposal of the adsorbed toxin. Therefore, (Fe(3-x)Ti(x))(1-δ)O(4) may be a promising sorbent in environmental applications. Herein, (Fe(3-x)Ti(x))(1-δ)O(4) is used as a magnetically separable sorbent for elemental mercury capture from the flue gas of coal-fired power plants. (Fe(2)Ti)(0.8)O(4) shows a moderate capacity (about 1.0 mg g(-1) at 250 °C) for elemental mercury capture in the presence of 1000 ppmv of SO(2). Meanwhile, the sorbent can be readily separated from the fly ash using magnetic separation, leaving the fly ash essentially free of sorbent and adsorbed mercury. PMID:21250644

  10. Mercury transformation and speciation in flue gases from anthropogenic emission sources: a critical review

    Science.gov (United States)

    Zhang, Lei; Wang, Shuxiao; Wu, Qingru; Wang, Fengyang; Lin, Che-Jen; Zhang, Leiming; Hui, Mulin; Yang, Mei; Su, Haitao; Hao, Jiming

    2016-02-01

    Mercury transformation mechanisms and speciation profiles are reviewed for mercury formed in and released from flue gases of coal-fired boilers, non-ferrous metal smelters, cement plants, iron and steel plants, waste incinerators, biomass burning and so on. Mercury in coal, ores, and other raw materials is released to flue gases in the form of Hg0 during combustion or smelting in boilers, kilns or furnaces. Decreasing temperature from over 800 °C to below 300 °C in flue gases leaving boilers, kilns or furnaces promotes homogeneous and heterogeneous oxidation of Hg0 to gaseous divalent mercury (Hg2+), with a portion of Hg2+ adsorbed onto fly ash to form particulate-bound mercury (Hgp). Halogen is the primary oxidizer for Hg0 in flue gases, and active components (e.g., TiO2, Fe2O3, etc.) on fly ash promote heterogeneous oxidation and adsorption processes. In addition to mercury removal, mercury transformation also occurs when passing through air pollution control devices (APCDs), affecting the mercury speciation in flue gases. In coal-fired power plants, selective catalytic reduction (SCR) system promotes mercury oxidation by 34-85 %, electrostatic precipitator (ESP) and fabric filter (FF) remove over 99 % of Hgp, and wet flue gas desulfurization system (WFGD) captures 60-95 % of Hg2+. In non-ferrous metal smelters, most Hg0 is converted to Hg2+ and removed in acid plants (APs). For cement clinker production, mercury cycling and operational conditions promote heterogeneous mercury oxidation and adsorption. The mercury speciation profiles in flue gases emitted to the atmosphere are determined by transformation mechanisms and mercury removal efficiencies by various APCDs. For all the sectors reviewed in this study, Hgp accounts for less than 5 % in flue gases. In China, mercury emission has a higher Hg0 fraction (66-82 % of total mercury) in flue gases from coal combustion, in contrast to a greater Hg2+ fraction (29-90 %) from non-ferrous metal smelting, cement and

  11. Mechanisms of mercury bioremediation.

    Science.gov (United States)

    Essa, A M M; Macaskie, L E; Brown, N L

    2002-08-01

    Mercury is one of the most toxic heavy metals, and has significant industrial and agricultural uses. These uses have led to severe localized mercury pollution. Mercury volatilization after its reduction to the metallic form by mercury-resistant bacteria has been reported as a mechanism for mercury bioremediation [Brunke, Deckwer, Frischmuth, Horn, Lunsdorf, Rhode, Rohricht, Timmis and Weppen (1993) FEMS Microbiol. Rev. 11, 145-152; von Canstein, Timmis, Deckwer and Wagner-Dobler (1999) Appl. Environ. Microbiol. 65, 5279-5284]. The reduction/volatilization system requires to be studied further, in order to eliminate the escape of the metallic mercury into the environment. Recently we have demonstrated three different mechanisms for mercury detoxification in one organism, Klebsiella pneumoniae M426, which may increase the capture efficiency of mercury.

  12. 焦木素对苯酚吸附性能的研究%STUDY ABOUT ADSORPTION PROPERTIES OF PYROXYLIN FOR PHENOL

    Institute of Scientific and Technical Information of China (English)

    李丽敏; 彭学伟; 焦为成

    2001-01-01

    With pyroxy as an adsorbent,the adsorption of pyroxylin for phenol in sewage,the rate of adsorption,the capacity of adsorption and the effect of pH on the adsorption of phenol were studied.The resullts indicated that the pyroxylin had well properties of adsorption,the adsorption isotherms were conformed to Freundlich equation.

  13. Removal of Bisphenol A from Aqueous solutions using Single walled carbon nanotubes: Investigation of adsorption isotherms

    Directory of Open Access Journals (Sweden)

    Elnaz Iravani

    2013-09-01

    Results: The maximum adsorption capacity was found to be 71.42 mg/g. The results of our experiments showed that maximum adsorption capacity at equilibrium was achieved at t = 60 min and pH = 9. Moreover, increasing the initial concentration is associated with an increase in adsorption capacity until it becomes constant. Conclusion: The BPA adsorption on SWCNT follows Freundlich-Langmuir isotherm.

  14. Mercury's heart of iron

    International Nuclear Information System (INIS)

    The one spacecraft to visit Mercury, Mariner 10, made three passes in 1974-75 after flying by Venus en route. Now, more than a decade after its first-and-only spacecraft visit, planetary scientists have absorbed the data from that flight - and are posing new questions with answers that call for a return to Mercury. Mercury is a metallic planet

  15. Teor e capacidade máxima de adsorção de arsênio em Latossolos brasileiros Content and maximum capacity of arsenic adsorption in Brazilian Oxisols

    Directory of Open Access Journals (Sweden)

    Mari Lucia Campos

    2007-12-01

    Full Text Available A alta toxicidade do As aos animais e humanos e a possibilidade de existência de grande número de áreas contaminadas tornam imprescindível o conhecimento do teor semitotal em solos ditos não-contaminados e dos processos de adsorção do As em solos de carga variável. O objetivo deste trabalho foi determinar o teor e a capacidade máxima de adsorção de As (CMADS AS em Latossolos. O teor total foi determinado pelo método USEPA 3051A, e a CMADS As, com auxílio de isotermas de Langmuir com base nos valores de adsorção obtidos em dose de As (0, 90, 190, 380, 760 e 1.150 µmol L-1 (relação solo:solução final = 1:100, a pH 5,5 e força iônica de 15 mmol L-1. Os 17 Latossolos apresentaram teor médio total de As de 5,92 mg kg-1 e CMADS As média de 2.013 mg kg-1. O teor de argila e os óxidos de Fe e Al apresentaram influência positiva na CMADS As.In view of the toxicity of As for man and animals and the possibility of existence of a great number of contaminated areas it is imperative to know the total As content in soils considered uncontaminated and about As sorption processes in soils of variable charge. The objective of this work was to determine the total content and maximum capacity of As adsorption (CMADS As in Oxisols. The total content was determined by the USEPA 3051A method. The cmADS As was determined by the Langmuir Isotherms using six solution concentrations (0, 0.09, 0.19, 0.38, 0.76, 1.15 mmol L-1 (1:100 soil: solution ratio, pH values 5.5 and ionic strength 15 mmol L-1. In the 17 Oxisols the average total As content was 5.92 mg kg-1 and mean cmADS As was 2.013 mg kg-1. Clay, and Fe and Al oxides content influenced cmADSs positively.

  16. Global Trends in Mercury Management

    OpenAIRE

    Kim, Dae-Seon; Choi, Kyunghee

    2012-01-01

    The United Nations Environmental Program Governing Council has regulated mercury as a global pollutant since 2001 and has been preparing the mercury convention, which will have a strongly binding force through Global Mercury Assessment, Global Mercury Partnership Activities, and establishment of the Open-Ended Working Group on Mercury. The European Union maintains an inclusive strategy on risks and contamination of mercury, and has executed the Mercury Export Ban Act since December in 2010. T...

  17. Adsorption of D113 Resin for Dysprosium(Ⅲ)

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The adsorption behavior and mechanism of D113 resin for Dy(Ⅲ) was investigated by using the method of resin adsorption. Experimental results show that the optimum medium pH of adsorption of D113 resin for Dy3+ is pH=6.00 in the HAc-NaAc medium. The static adsorption capacity of D113 resin for Dy3+chemical analysis and IR spectra.

  18. Adsorption and Desorption of Methiopyrsulfuron in Soils

    Institute of Scientific and Technical Information of China (English)

    WU Chun-Xian; WANG Jin-Jun; ZHANG Su-Zhi; ZHANG Zhong-Ming

    2011-01-01

    Methiopyrsulfuron is a new low-rate sulfonylurea herbicide for weed control in wheat; however, there is a lack of published information on its behavior in soils. In this study, methiopyrsulfuron adsorption and desorption were measured in seven soils sampled from Heilongjiang, Shandong, Jiangxi, Sichuan, Anhui, and Chongqing provinces of China using a batch equilibrium method. The Freundlich equation was used to described its adsorption and desorption. Adsorption isotherms were nonlinear with the values of Kf-ads, the Freundlich empirical constant indicative of the adsorption capacity,ranging from 0.75 to 2.46, suggesting that little of this herbicide was adsorbed by any of the seven soils. Soil pH and organic matter content (OM) were the main factors influencing adsorption; adsorption was negatively correlated with pH and positively correlated with OM. Methiopyrsulfuron desorption was hysteretic on the soils with high OM content and low pH.

  19. ADSORPTION AND RELEASING PROPERTIES OF BEAD CELLULOSE

    Institute of Scientific and Technical Information of China (English)

    A. Morales; E. Bordallo; V. Leon; J. Rieumont

    2004-01-01

    The adsorption of some dyes on samples of bead cellulose obtained in the Unit of Research-Production "Cuba 9"was studied. Methylene blue, alizarin red and congo red fitted the adsorption isotherm of Langmuir. Adsorption kinetics at pH = 6 was linear with the square root of time indicating the diffusion is the controlling step. At pH = 12 a non-Fickian trend was observed and adsorption was higher for the first two dyes. Experiments carried out to release the methylene blue occluded in the cellulose beads gave a kinetic behavior of zero order. The study of cytochrome C adsorption was included to test a proteinic material. Crosslinking of bead cellulose was performed with epichlorohydrin decreasing its adsorption capacity in acidic or alkaline solution.

  20. Effect of piezoelectric material on hydrogen adsorption

    Energy Technology Data Exchange (ETDEWEB)

    Li, Xuan [Department of Materials Science and Engineering, Michigan Technological University, 1400 Townsend Drive, Houghton, MI, 49931 (United States); Civil and Environmental Engineering School, University of Science and Technology Beijing, 30 Xueyuan Road, Haidian District, Beijing, 100083 (China); Hwang, Jiann-Yang; Shi, Shangzhao; Sun, Xiang; Zhang, Zheng [Department of Materials Science and Engineering, Michigan Technological University, 1400 Townsend Drive, Houghton, MI, 49931 (United States)

    2010-09-15

    In hydrogen storage applications, the primary issue for physisorption of hydrogen onto solid-state materials is the weak interaction force between hydrogen molecules and the adsorbents. It is found that enhanced adsorption can be obtained under an external electric field, because it appears the electric field increases the hydrogen adsorption energy. Experiments were carried out to determine hydrogen adsorption on activated carbon using the piezoelectric material PMN-PT as the charge supplier under hydrogen pressure. Results indicate that more than 20% hydrogen adsorption enhancement was obtained. Parameters related to hydrogen adsorption enhancement include the amount of the charge and temperature. Higher voltage and lower temperature promote the increase of adsorption capacity but room temperature results are very encouraging. (author)

  1. Adsorption of octylamine on titanium dioxide

    International Nuclear Information System (INIS)

    Processes of adsorption and desorption of a model active substance (octylamine) on the surface of unmodified titanium dioxide (E 171) have been performed. The effects of concentration of octylamine and time of the process on the character of adsorption have been studied and the efficiency of the adsorption/desorption has been determined. The samples obtained have been studied by X-ray diffraction. The nitrogen adsorption/desorption isotherms, particle size distribution and absorption capacities of water, dibutyl phthalate and paraffin oil have been determined. The efficiency of octylamine adsorption on the surface of the titanium dioxide has been found positively correlated with the concentration of octylamine in the initial solution. The desorption of octylamine has decreased with increasing concentration of this compound adsorbed. For octylamine in low concentrations the physical adsorption has been found to dominate, which is desirable when using TiO2 in the production of pharmaceuticals.

  2. Capacidade de adsorção de fósforo em solos de várzea do Estado do Rio Grande do Sul Phosphorus adsorption capacity in lowland soils of Rio Grande do Sul State

    Directory of Open Access Journals (Sweden)

    Sidnei Kuster Ranno

    2007-02-01

    highly reactive elements such as phosphorus. Low-crystallinity forms of iron oxides and hydroxides become predominant with time. They could be the most important components in phosphorus adsorption during dry periods, and could control phosphorus release after flooding. The objective of this study was to evaluate the maximum phosphorus adsorption capacity (MPAC of some lowland soils in Rio Grande do Sul State (RS, Brazil and relate it with soil chemical and physical properties. Soil samples from 16 different areas in RS with widely varied soil chemical and physical properties were collected from the surface layer (0-20 cm. They were air-dried, sieved (2 mm, and the MPAC measured using adsorption isotherms. Each soil was kept in contact with increasing levels of P (0, 50, 100, 200, 300, 600, 900, and 1.800 mg kg-1 of P soil for 16 hours. The equilibrium P in the solution was determined and the data fit to the Langmuir equation. The MPAC varied considerably among the RS lowland soils (from 71 to 933 mg kg-1 of P; the variation was significantly correlated with the clay, organic matter and iron oxide contents extracted by dithionite and ammonium oxalate. The different MPAC affected the phosphorous doses necessary to increase available phosphorous by the Mehlich-1extractant in lowland soils.

  3. Determination of mercury by substoichiometric isotope dilution analysis

    Energy Technology Data Exchange (ETDEWEB)

    Sandhya, D. (Dept. of Chemistry, Indian Inst. of Tech., Madras (India)); Subramanian, M.S. (Dept. of Chemistry, Indian Inst. of Tech., Madras (India))

    1994-01-01

    A radiometric method based on Substoichiometric Isotope Dilution Analysis has been developed for the determination of trace amounts of mercury using [alpha]-Thiopicolin-o-anisylamide (TPA) as a substoichiometric reagent. A preconcentration procedure has also been developed based on the adsorption of mercury(II) as a dithizone complex onto microcrystalline naphthalene which when used in conjunction with the proposed radiometric method enhances its sensitivity and selectivity. As low as 0.2 [mu]g of mercury could be determined in an aqueous phase volume of 80 ml. The method has been successfully applied for the determination of trace amounts of mercury in city waste incineration ash, zinc metal and cadmium oxide samples. (orig.)

  4. Changing patterns in the use, recycling, and material substitution of mercury in the United States

    Science.gov (United States)

    Wilburn, David R.

    2013-01-01

    Environmental concerns have led to numerous regulations that have dramatically decreased the reported production and use of mercury in the United States since the 1980s. Government legislation and subsequent industry actions have led to increased collection of mercury-containing materials and the recovery of mercury through recycling. Mercury emissions have been reduced and effective alternatives to mercury products have been developed for many applications. This study updates and quantifies the changes in demand, supply, use, and material flow for mercury in various sectors in the United States that have taken place since 1996. Nearly all primary mercury produced in the United States is derived as a byproduct of processing of gold and silver ore in Nevada. Since 2001, annual production of mercury from gold and silver mining in Nevada has decreased by 22 percent overall because ore from greater depths containing low grade mercury is recovered, and mercury emissions from this source have decreased by 95 percent as a result of increased regulation and improved collection and suppression technology. The distribution of consumption of mercury in the United States has changed as a result of regulation (elimination of large-scale mercury use in the paint and battery sectors), reduction by consumers (decommissioning of mercury-cell chloralkali manufacturing capacity), and technological advances (improvements in dental, lighting, and wiring sectors). Mercury use in the chloralkali sector, the leading end-use sector in the United States in 1996, has declined by 98 percent from 136 metric tons (t) in 1996 to about 0.3 t in 2010 because of increased processing and recycling efficiencies and plant closures or conversion to other technologies. As plants were closed, mercury recovered from the infrastructure of decommissioned plants has been exported, making the United States a net exporter of mercury, even though no mercury has been produced as the primary product from mines in

  5. RECOVERY OF MERCURY FROM CONTAMINATED PRIMARY AND SECONDARY WASTES

    International Nuclear Information System (INIS)

    Effective removal of mercury contamination from water is a complex and difficult problem. In particular, mercury treatment of natural waters is difficult because of the low regulatory standards. For example, the Environmental Protection Agency has established a national ambient water quality standard of 12 parts-per-trillion (ppt), whereas the standard is 1.8 ppt in the Great Lakes Region. In addition, mercury is typically present in several different forms, but sorption processes are rarely effective with more than one or two of these forms. To meet the low regulatory discharge limits, a sorption process must be able to address all forms of mercury present in the water. One approach is to apply different sorbents in series depending on the mercury speciation and the regulatory discharge limits. Four new sorbents have been developed to address the variety of mercury species present in industrial discharges and natural waters. Three of these sorbents have been field tested on contaminated creek water at the Y-12 Plant. Two of these sorbents have demonstrated very high removal efficiencies for soluble mercury species, with mercury concentrations at the outlet of a pilot-scale system less than 12 ppt for as long as six months. The other sorbent tested at the Y-12 Plant is targeted at colloidal mercury that is not removed by standard sorption or filtration processes. At the Y-12 Plant, colloidal mercury appears to be associated with iron, so a sorbent that removes mercury-iron complexes in the presence of a magnetic field was evaluated. Field results indicate good removal of this mercury fraction from the Y-12 waters. In addition, this sorbent is easily regenerated by simply removing the magnetic field and flushing the columns with water. The fourth sorbent is still undergoing laboratory development, but results to date indicate exceptionally high mercury sorption capacity. The sorbent is capable of removing all forms of mercury typically present in natural and

  6. Modeling of mercury speciation and capture in coal-fired flue gas

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Heyang; Ma, Zhanhua; Lu, Pisi [SmartBurn LLC, Madison, WI (United States); Cao, Yan; Pan, Wei-Ping [Western Kentucky Univ., Bowling Green, KY (United States). ICSET

    2013-07-01

    A 3D computational fluid dynamics (CFD) modeling tool was developed to model the mercury speciation and capture processes in coal-fired flue gas, including gaseous mercury oxidation and adsorption of mercury by the particulate matter. This CFD modeling tool was then applied to predicting enhanced mercury oxidation and capture by HBr injection in a slipstream reactor. The reaction rate constants of the mercury oxidation by HBr are extracted from the slipstream reactor testing data from the ICSET of Western Kentucky University. The modeling results show good agreement with the testing data and reasonable trends under different conditions. This CFD modeling tool can be either used to design a new mercury control system with higher efficiency and lower operating cost or to improve the performance of an existing system.

  7. [Removal Characteristics of Elemental Mercury by Mn-Ce/molecular Sieve].

    Science.gov (United States)

    Tan, Zeng-qiang; Niu, Guo-ping; Chen, Xiao-wen; An, Zhen

    2015-06-01

    The impregnation method was used to support molecular sieve with active manganese and cerium components to obtain a composite molecular sieve catalyst. The mercury removal performance of the catalyst was studied with a bench-scale setup. XPS analysis was used to characterize the sample before and after the modification in order to study the changes in the active components of the catalyst prepared. The results showed that the catalyst carrying manganese and cerium components had higher oxidation ability of elemental mercury in the temperature range of 300 degrees C - 450 degrees C, especially at 450 degrees C, the oxidation efficiency of elemental mercury was kept above 80%. The catalyst had more functional groups that were conducive to the oxidation of elemental mercury, and the mercury removal mainly depended on the chemical adsorption. The SO2 and NO in flue gas could inhibit the oxidation of elemental mercury to certain extent. PMID:26387298

  8. Adsorption characteristics of siloxanes in landfill gas by the adsorption equilibrium test

    Energy Technology Data Exchange (ETDEWEB)

    Nam, Sangchul; Namkoong, Wan [Department of Environmental Engineering, Konkuk University, Hwayang-Dong, Gwangjin-Gu, Seoul 143-701 (Korea, Republic of); Kang, Jeong-Hee; Park, Jin-Kyu [Department of Environmental Engineering, Anyang University, Anyang 5-Dong, Manan-Gu, Anyang-Si, Gyeonggi-Do 430-714 (Korea, Republic of); Lee, Namhoon, E-mail: nhlee@anyang.ac.kr [Department of Environmental Engineering, Anyang University, Anyang 5-Dong, Manan-Gu, Anyang-Si, Gyeonggi-Do 430-714 (Korea, Republic of)

    2013-10-15

    Highlights: • Equilibrium test was attempted to evaluate adsorption characteristics of siloxane. • L2 had higher removal efficiency in carbon compared to noncarbon adsorbents. • Total adsorption capacity of siloxane was 300 mg/g by coal activated carbon. • Adsorption characteristics rely on size of siloxane molecule and adsorbent pore. • Conversion of siloxane was caused by adsorption of noncarbon adsorbents. - Abstract: Due to the increase in energy cost by constantly high oil prices and the obligation to reduce greenhouse effect gases, landfill gas is frequently used as an alternative energy source for producing heat and electricity. Most of landfill gas utility facilities, however, are experiencing problems controlling siloxanes from landfill gas as their catalytic oxidizers are becoming fouled by silicon dioxide dust. To evaluate adsorption characteristics of siloxanes, an adsorption equilibrium test was conducted and parameters in the Freundlich and Langmuir isotherms were analyzed. Coconut activated carbon (CA1), coal activated carbon (CA2), impregnated activated carbon (CA3), silicagel (NCA1), and activated alumina (NCA2) were used for the adsorption of the mixed siloxane which contained hexamethyldisiloxane (L2), octamethylcyclotetrasiloxane (D4), and decamethylcyclopentasiloxane (D5). L2 had higher removal efficiency in noncarbon adsorbents compared to carbon adsorbents. The application of Langmuir and Freundlich adsorption isotherm demonstrated that coconut based CA1 and CA3 provided higher adsorption capacity on L2. And CA2 and NCA1 provided higher adsorption capacity on D4 and D5. Based on the experimental results, L2, D4, and D5 were converted by adsorption and desorption in noncarbon adsorbents. Adsorption affinity of siloxane is considered to be affect by the pore size distribution of the adsorbents and by the molecular size of each siloxane.

  9. Adsorption Rate Models for Multicomponent Adsorption Systems

    Institute of Scientific and Technical Information of China (English)

    姚春才

    2004-01-01

    Three adsorption rate models are derived for multicomponent adsorption systems under either pore diffusion or surface diffusion control. The linear driving force (LDF) model is obtained by assuming a parabolic intraparticle concentration profile. Models I and Ⅱ are obtained from the parabolic concentration layer approximation. Examples are presented to demonstrate the usage and accuracy of these models. It is shown that Model I is suitable for batch adsorption calculations and Model Ⅱ provides a good approximation in fixed-bed adsorption processes while the LDF model should not be used in batch adsorption and may be considered acceptable in fixed-bed adsorption where the parameter Ti is relatively large.

  10. Adsorption of Congo Red onto Lignocellulose/Montmorillonite Nanocomposite

    Institute of Scientific and Technical Information of China (English)

    ZHAO Yahong; XUE Zhenhua; WANG Ximing; WANG Li; WANG Aiqin

    2012-01-01

    Lignocellulose/montmorillonite (LNC/MMT) nanocomposites were prepared and characterized by FTIR and XRD.The adsorption of congo red (CR) on LNC/MMT nanocomposite was studied in detail.The effects of contact temperature,pH value of the dye solutions,contact time and concentration of dye solutions on the adsorption capacities of lignocellulose (LNC),montmorillonite (MMT) and the nanocomposite were investigated.The adsorption kinetics and isotherms and adsorption thermodynamics of the nanocomposite for CR were also studied.The results show that the adsorption capacity of LNC/MMT nanocomosite is higher than that of LNC and MMT.All the adsorption processes fit very well with the pseudo-second-order and the Langmuir equation.From thermodynamic studies,it is seen that the adsorption is spontaneous and endothermic.

  11. Process for low mercury coal

    Science.gov (United States)

    Merriam, Norman W.; Grimes, R. William; Tweed, Robert E.

    1995-01-01

    A process for producing low mercury coal during precombustion procedures by releasing mercury through discriminating mild heating that minimizes other burdensome constituents. Said mercury is recovered from the overhead gases by selective removal.

  12. Adsorption and wetting.

    NARCIS (Netherlands)

    Schlangen, L.J.M.

    1995-01-01

    Adsorption and wetting are related phenomena. In order to improve knowledge of both and their relations, experiments, thermodynamics and a theoretical interpretation have been connected, starring n-alkanes.Starting from the Gibbs adsorption equation thermodynamic relations between vapour adsorption

  13. Removal of heavy metals from water by zeolite mineral chemically modified. Mercury as a particular case; Remocion de metales pesados del agua por mineral zeolitico quimicamente modificado. Mercurio como un caso particular

    Energy Technology Data Exchange (ETDEWEB)

    Gebremedhin H, T

    2002-07-01

    Research works on the removal of mercury from water by zeolite minerals show that a small quantity of this element is sorbed. In this work the mercury sorption from aqueous solutions in the presence and absence of Cu(l l), Ni(l l) and/or Zn(l l) by a Mexican zeolite mineral, natural and modified by cisteaminium chloride or cistaminium dichloride, was investigated in acidic p H. The zeolite minerals were characterized by X- Ray diffraction Ftir, scanning electron microscopy and semiquantitative elemental analysis (EDS), surface area analysis (BET) and thermogravimetric analysis (TGA). Mercury from aqueous solutions was quantified by Atomic absorption spectroscopy. The amount of sulphur on the zeolite samples treated with Na CI and modified with cisteaminium chloride (0.375 mmol/g) or cistaminium dichloride(0.475 mmol/g) was found to be higher than that of the zeolite minerals modified with cisteaminium chloride and cistaminium dichloride without treating them with Na CI. The amount of sulphur on the zeolite minerals modified with thiourea was the lowest. The diffusion coefficients and sorption isotherms for mercury were determined in the natural, treated with Na CI and, treated with Na CI and then modified with the cisteaminium chloride or cistaminium dichloride zeolite samples. The retention of mercury was the highest for the zeolite minerals treated Na CI and then modified with cisteaminium chloride or cistaminium dichloride, with adsorption capacity of 0.0511 and 0.0525 mmol Hg/g, respectively. In this research work, it was found that the retention of mercury by the modified minerals was not affected by the presence of Cu (Il), Zn(l l) y Ni (I l) under the experimental conditions. (Author)

  14. Mercury is Moon's brother

    International Nuclear Information System (INIS)

    The latest information on Mercury planet is presented obtained by studying the planet with the aid of radar and space vehicles. Rotation of Mercury about its axis has been discovered; within 2/3 of its year it executes a complete revolution about its axis. In images obtained by the ''Mariner-10'' Mercurys surface differs little from that of the Moon. The ''Mariner-10'' has also discovered the Mercurys atmosphere, which consists of extremely rarefied helium. The helium is continuously supplied to the planet by the solar wind. The Mercury's magnetic field has been discovered, whose strength is 35 x 10-4 at the Equator and 70 x 10-4 E at the poles. The inclination of the dipole axis to the Mercury's rotation axis is 7 deg

  15. Novel sandwich structure adsorptive membranes for removal of 4-nitrotoluene from water.

    Science.gov (United States)

    Guo, Yuexin; Jia, Zhiqian

    2016-11-01

    Novel sandwich PES-SPES/PS-PDVB/PTFE adsorptive membranes were prepared by a filtration/immersion precipitation method and employed for the removal of 4-nitrotoluene from water. The static adsorption thermodynamics, kinetics, dynamic adsorption/desorption and membrane reusability were investigated. The results showed that the Freundlich model describes the adsorption isotherm satisfactorily. With increased PS-PDVB content, the maximum static adsorption capacity, partition coefficient, apparent adsorption rate constant, and dynamic adsorption capacity all significantly increased. The sandwich membranes showed much higher removal efficiency and adsorption capacity than those of mixed matrix membranes. With respect to dynamics adsorption/desorption, the sandwich membranes exhibited excellent reusability, with a removal efficiency greater than 95% even after five recycles. PMID:27322899

  16. Aplicación del Modelo de Bohart y Adams en la Remoción de Mercurio de Drenajes de Minería por Adsorción con Carbón Activado Application of the Bohart and Adams Model in the Removal of Mercury from Mine Drainage by Adsorption with Activated Carbon

    Directory of Open Access Journals (Sweden)

    Hugo A Rojas

    2012-01-01

    Full Text Available Se aplica el modelo de Bohart y Adams al proceso de remoción de mercurio de los drenajes de minería por adsorción con carbón activado en columnas de lecho fijo. Para ello se analizaron diferentes drenajes de minas de carbón de Guachetá en Colombia y se simularon en el laboratorio las condiciones reales de vertido de los drenajes. Establecidas las condiciones de funcionamiento óptimo de la columna, se realizó un estudio detallado de curvas de ruptura, a través del modelo de Bohart y Adams, para determinar la vida útil del material adsorbente y la efectividad del método para la remoción del ion metálico. Se estableció que el tiempo de ruptura es de 20 min. y que la columna con el mejor rendimiento tiene 1.7 cm de diámetro y 2 cm de altura del lecho, bajo las condiciones de estudio. El modelo usado describió la parte inicial de la curva de ruptura y los parámetros obtenidos permitieron diseñar y optimizar el funcionamiento de sistemas de adsorción en lecho fijo para la remoción de iones Hg²+ de efluentes acuosos.The model of Bohart and Adams was applied to the process of removal of mercury from mine drainage by adsorption with activated carbon in fixed bed columns. For this several drains from coal mines of Guachetá in Colombia, were studied. Once the optimum operating conditions of the column are established, a detailed study of breakthrough curves using the Bohart and Adams model was done, to determine the lifetime of the adsorbent material and the effectiveness of the method for removal the metal ions. It was established that the breakthrough time was 20 min. and the column with the best performance was 1.7 cm in diameter and 2 cm bed length, under the study conditions. The model described the initial part of the breakthrough curve and the parameters of the model allow designing and optimizing the performance of fixed bed adsorption systems for the removal of Hg²+ ions fro aqueous mine wastes.

  17. Fluorocarbon Adsorption in Hierarchical Porous Frameworks

    Energy Technology Data Exchange (ETDEWEB)

    Motkuri, Radha K.; Annapureddy, Harsha V.; Vijayakumar, M.; Schaef, Herbert T.; Martin, P F.; McGrail, B. Peter; Dang, Liem X.; Krishna, Rajamani; Thallapally, Praveen K.

    2014-07-09

    The adsorption behavior of a series of fluorocarbon derivatives was examined on a set of microporous metal organic framework (MOF) sorbents and another set of hierarchical mesoporous MOFs. The microporous M-DOBDC (M = Ni, Co) showed a saturation uptake capacity for R12 of over 4 mmol/g at a very low relative saturation pressure (P/Po) of 0.02. In contrast, the mesoporous MOF MIL-101 showed an exceptionally high uptake capacity reaching over 14 mmol/g at P/Po of 0.4. Adsorption affinity in terms of mass loading and isosteric heats of adsorption were found to generally correlate with the polarizability of the refrigerant with R12 > R22 > R13 > R14 > methane. These results suggest the possibility of exploiting MOFs for separation of azeotropic mixtures of fluorocarbons and use in eco-friendly fluorocarbon-based adsorption cooling and refrigeration applications.

  18. Peru Mercury Inventory 2006

    Science.gov (United States)

    Brooks, William E.; Sandoval, Esteban; Yepez, Miguel A.; Howard, Howell

    2007-01-01

    In 2004, a specific need for data on mercury use in South America was indicated by the United Nations Environmental Programme-Chemicals (UNEP-Chemicals) at a workshop on regional mercury pollution that took place in Buenos Aires, Argentina. Mercury has long been mined and used in South America for artisanal gold mining and imported for chlor-alkali production, dental amalgam, and other uses. The U.S. Geological Survey (USGS) provides information on domestic and international mercury production, trade, prices, sources, and recycling in its annual Minerals Yearbook mercury chapter. Therefore, in response to UNEP-Chemicals, the USGS, in collaboration with the Economic Section of the U.S. Embassy, Lima, has herein compiled data on Peru's exports, imports, and byproduct production of mercury. Peru was selected for this inventory because it has a 2000-year history of mercury production and use, and continues today as an important source of mercury for the global market, as a byproduct from its gold mines. Peru is a regional distributor of imported mercury and user of mercury for artisanal gold mining and chlor-alkali production. Peruvian customs data showed that 22 metric tons (t) of byproduct mercury was exported to the United States in 2006. Transshipped mercury was exported to Brazil (1 t), Colombia (1 t), and Guyana (1 t). Mercury was imported from the United States (54 t), Spain (19 t), and Kyrgyzstan (8 t) in 2006 and was used for artisanal gold mining, chlor-alkali production, dental amalgam, or transshipment to other countries in the region. Site visits and interviews provided information on the use and disposition of mercury for artisanal gold mining and other uses. Peru also imports mercury-containing batteries, electronics and computers, fluorescent lamps, and thermometers. In 2006, Peru imported approximately 1,900 t of a wide variety of fluorescent lamps; however, the mercury contained in these lamps, a minimum of approximately 76 kilograms (kg), and in

  19. Sorption of mercury (II) and methyl mercury from waters by tannin sorbents, using 203 Hg As radiotracer

    International Nuclear Information System (INIS)

    Sorption of mercury (II) and methyl mercury by two tannin sorbents was investigated using radiotracers. High sorption capacities for mercury are registered for both sorbents at pH 7. For Eucalyptus Saligna Sm sorbent (ETS) maximum sorption capacity was 1.2 +- 0.2 mmol/g and for Lysiloma latisiliqua B. sorbent (LTS) was 8.5 +- 0.2 mmol/g. Methylmercury sorption maximum was recorded at pH 4 and in buffered solutions at pH 2, this specie can be recovered in presence of mercury (II). Influence of different ions present in water was examined. High recoveries were reported for ETS in tap water samples but a decrease of uptake is observed for seawater

  20. Accidental inhalation of mercury vapour: respiratory and toxicologic consequences.

    OpenAIRE

    Lien, D. C.; Todoruk, D. N.; Rajani, H. R.; Cook, D A; Herbert, F. A.

    1983-01-01

    Four adults, including a pregnant woman, and three children were admitted to hospital following accidental exposure to mercury vapour produced by heating mercury-gold amalgam. Initial symptoms and signs included a paroxysmal cough, dyspnea, chest pain, tachypnea, nausea, vomiting, fever and leukocytosis. Pulmonary function testing performed on the second day after exposure revealed air-flow obstruction and minor restrictive defects in three patients. The diffusing capacity of the lung for car...

  1. Phosphate adsorption on aluminum-coordinated functionalized macroporous–mesoporous silica: Surface structure and adsorption behavior

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Al-coordinated functionalized macroporous–mesoporous silica for phosphate removal. • It had the maximum adsorption capacity of 23.59 mg P/g. • Over 95% of the final adsorption capacity reached in the first 1 min. - Abstract: In this study, Al(III)-coordinated diamino-functionalized macroporous–mesoporous silica was synthesized and characterized by X-ray diffraction, N2 adsorption–desorption, Fourier transform infrared spectroscopy, scanning and transmission electron microscopy. Because of well-defined and interconnecting macroporous–mesoporous networks, the resulting adsorbent (MM-SBA) exhibited a significantly better phosphate adsorption performance and faster removal rate, as compared with the mesoporous adsorbent (M-SBA). Based on the Freundlich and Langmuir models, the phosphate adsorption capacity and the maximum adsorption capacity of MM-SBA were 7.99 mg P/g and 23.59 mg P/g, respectively. In the kinetic study of MM-SBA, over 95% of its final adsorption capacity reached in the first 1 min; whereas that of M-SBA was less than 79%

  2. Phosphate adsorption on aluminum-coordinated functionalized macroporous–mesoporous silica: Surface structure and adsorption behavior

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Weiya [Department of Chemistry, Jinan University, Guangzhou 510632 (China); Department of Materials Science and Engineering, Taizhou University, Linhai 317000 (China); Li, Dan [Environmetal Engineering, School of Engineering and Information Technology, Murdoch University, Murdoch, Western Australia 6150 (Australia); Zhu, Yi; Xu, Kai; Li, Jianqiang [Department of Chemistry, Jinan University, Guangzhou 510632 (China); Han, Boping [Institute of Hydrobiology, Jinan University, Guangzhou 510460 (China); Zhang, Yuanming, E-mail: tzhangym@jnu.edu.cn [Department of Chemistry, Jinan University, Guangzhou 510632 (China)

    2013-12-15

    Graphical abstract: - Highlights: • Al-coordinated functionalized macroporous–mesoporous silica for phosphate removal. • It had the maximum adsorption capacity of 23.59 mg P/g. • Over 95% of the final adsorption capacity reached in the first 1 min. - Abstract: In this study, Al(III)-coordinated diamino-functionalized macroporous–mesoporous silica was synthesized and characterized by X-ray diffraction, N{sub 2} adsorption–desorption, Fourier transform infrared spectroscopy, scanning and transmission electron microscopy. Because of well-defined and interconnecting macroporous–mesoporous networks, the resulting adsorbent (MM-SBA) exhibited a significantly better phosphate adsorption performance and faster removal rate, as compared with the mesoporous adsorbent (M-SBA). Based on the Freundlich and Langmuir models, the phosphate adsorption capacity and the maximum adsorption capacity of MM-SBA were 7.99 mg P/g and 23.59 mg P/g, respectively. In the kinetic study of MM-SBA, over 95% of its final adsorption capacity reached in the first 1 min; whereas that of M-SBA was less than 79%.

  3. Adsorption of thorium from aqueous solutions by perlite.

    Science.gov (United States)

    Talip, Z; Eral, M; Hiçsönmez, U

    2009-02-01

    The use of expanded perlite for the adsorption of thorium from aqueous solution by batch technique is presented. The effects of particle size, pH of the solution, initial thorium concentration, shaking time, V/m ratio and temperature were determined. It was found that the adsorption capacity increases by the increase in the pH of the suspensions. The rate of thorium adsorption on expanded perlite was observed to be fast in the first hour of the reaction time. Adsorption isotherms were expressed by Langmuir and Freundlich adsorption models and the adsorption experiments conducted at 30 +/- 1 degrees C showed that the adsorption isotherms correlated well with the Langmuir model. From the adsorption data, thermodynamic parameters such as DeltaG(o), DeltaH(o) and DeltaS(o) were calculated as a function of temperature.

  4. Competitive adsorption of heavy metals onto sesame straw biochar in aqueous solutions.

    Science.gov (United States)

    Park, Jong-Hwan; Ok, Yong Sik; Kim, Seong-Heon; Cho, Ju-Sik; Heo, Jong-Soo; Delaune, Ronald D; Seo, Dong-Cheol

    2016-01-01

    Objective of this research was to evaluate adsorption of heavy metals in mono and multimetal forms onto sesame straw biochar (SSB). Competitive sorption of metals by SSB has never been reported previously. The maximum adsorption capacities (mgg(-1)) of metals by SSB were in the order of Pb (102)≫Cd (86)≫Cr (65)>Cu (55)≫Zn (34) in the monometal adsorption isotherm and Pb (88)≫Cu (40)≫Cr (21)>Zn (7)⩾Cd (5) in the multimetal adsorption isotherm. Based on data obtained from the distribution coefficients, Freundlich and Langmuir adsorption models, and three-dimensional simulation, multimetal adsorption behaviors differed from monometal adsorption due to competition. Especially, during multimetal adsorption, Cd was easily exchanged and substituted by other metals. Further competitive adsorption studies are necessary in order to accurately estimate the heavy metal adsorption capacity of biochar in natural environments.

  5. Modeling Mercury in Proteins

    Energy Technology Data Exchange (ETDEWEB)

    Smith, Jeremy C [ORNL; Parks, Jerry M [ORNL

    2016-01-01

    Mercury (Hg) is a naturally occurring element that is released into the biosphere both by natural processes and anthropogenic activities. Although its reduced, elemental form Hg(0) is relatively non-toxic, other forms such as Hg2+ and, in particular, its methylated form, methylmercury, are toxic, with deleterious effects on both ecosystems and humans. Microorganisms play important roles in the transformation of mercury in the environment. Inorganic Hg2+ can be methylated by certain bacteria and archaea to form methylmercury. Conversely, bacteria also demethylate methylmercury and reduce Hg2+ to relatively inert Hg(0). Transformations and toxicity occur as a result of mercury interacting with various proteins. Clearly, then, understanding the toxic effects of mercury and its cycling in the environment requires characterization of these interactions. Computational approaches are ideally suited to studies of mercury in proteins because they can provide a detailed picture and circumvent issues associated with toxicity. Here we describe computational methods for investigating and characterizing how mercury binds to proteins, how inter- and intra-protein transfer of mercury is orchestrated in biological systems, and how chemical reactions in proteins transform the metal. We describe quantum chemical analyses of aqueous Hg(II), which reveal critical factors that determine ligand binding propensities. We then provide a perspective on how we used chemical reasoning to discover how microorganisms methylate mercury. We also highlight our combined computational and experimental studies of the proteins and enzymes of the mer operon, a suite of genes that confers mercury resistance in many bacteria. Lastly, we place work on mercury in proteins in the context of what is needed for a comprehensive multi-scale model of environmental mercury cycling.

  6. Modeling Mercury in Proteins.

    Science.gov (United States)

    Parks, J M; Smith, J C

    2016-01-01

    Mercury (Hg) is a naturally occurring element that is released into the biosphere both by natural processes and anthropogenic activities. Although its reduced, elemental form Hg(0) is relatively nontoxic, other forms such as Hg(2+) and, in particular, its methylated form, methylmercury, are toxic, with deleterious effects on both ecosystems and humans. Microorganisms play important roles in the transformation of mercury in the environment. Inorganic Hg(2+) can be methylated by certain bacteria and archaea to form methylmercury. Conversely, bacteria also demethylate methylmercury and reduce Hg(2+) to relatively inert Hg(0). Transformations and toxicity occur as a result of mercury interacting with various proteins. Clearly, then, understanding the toxic effects of mercury and its cycling in the environment requires characterization of these interactions. Computational approaches are ideally suited to studies of mercury in proteins because they can provide a detailed molecular picture and circumvent issues associated with toxicity. Here, we describe computational methods for investigating and characterizing how mercury binds to proteins, how inter- and intraprotein transfer of mercury is orchestrated in biological systems, and how chemical reactions in proteins transform the metal. We describe quantum chemical analyses of aqueous Hg(II), which reveal critical factors that determine ligand-binding propensities. We then provide a perspective on how we used chemical reasoning to discover how microorganisms methylate mercury. We also highlight our combined computational and experimental studies of the proteins and enzymes of the mer operon, a suite of genes that confer mercury resistance in many bacteria. Lastly, we place work on mercury in proteins in the context of what is needed for a comprehensive multiscale model of environmental mercury cycling. PMID:27497164

  7. Adsorption of Iminodiacetic Acid Resin for Lutetium

    Institute of Scientific and Technical Information of China (English)

    熊春华; 姚彩萍; 王惠君

    2004-01-01

    The adsorption behavior and mechanism of a novel chelate resin,iminodiacetic acid resin(IDAAR) for Lu(Ⅲ) were investigated.The statically saturated adsorption capacity is 210.8 mg·g-1 at 298 K in HAc-NaAc medium.The Lu(Ⅲ) adsorbed on IDAAR can be eluted by 0.5 mol·L-1 HCl and the elution percentage reaches 96.5%.The resin can be regenerated and reused without obvious decrease in adsorption capacity.The apparent adsorption rate constant is k298=2.0×10-5 s-1.The adsorption behavior of IDAAR for Lu(Ⅲ) obeys the Freundlich isotherm.The thermodynamic adsorption parameters,enthalpy change ΔH,free energy change ΔG and entropy change ΔS of IDAAR for Lu(Ⅲ) are 13.1 kJ·mol-1,-1.37 kJ·mol-1 and 48.4 J·mol-1·K-1,respectively.The apparent activation energy is Ea=31.3 kJ·mol-1.The molar coordination ratio of the functional group of IDAAR to Lu(Ⅲ) is about 3∶1.The adsorption mechanism of IDAAR for Lu(Ⅲ) was examined by chemical method and IR spectrometry.

  8. Nitrate Adsorption on Clay Kaolin: Batch Tests

    Directory of Open Access Journals (Sweden)

    Morteza Mohsenipour

    2015-01-01

    Full Text Available Soils possessing kaolin, gibbsite, goethite, and hematite particles have been found to have a natural capacity to attenuate pollution in aqueous phase. On the other hand, the hydroxyl group in soil increases anion exchange capacity under a low pH condition. The main objective of this paper was to evaluate effects of kaolin on nitrate reduction under acidic condition. In order to analyze the kaolin adsorption behaviour under various conditions, four different concentrations of nitrate, 45, 112.5, 225, and 450 mgNO3-/L, with a constant pH equal to 2, constant temperature equal to 25°C, and exposure period varying from 0 to 150 minutes were considered. The capacity of nitrate adsorption on kaolin has also been studied involving two well-known adsorption isotherm models, namely, Freundlich and Longmuir. The results revealed that approximately 25% of the nitrate present in the solution was adsorbed on clay kaolin. The laboratory experimental data revealed that Freundlich adsorption isotherm model was more accurate than Longmuir adsorption model in predicting of nitrate adsorption. Furthermore, the retardation factor of nitrate pollution in saturated zone has been found to be approximately 4 in presence of kaolin, which indicated that kaolin can be used for natural scavenger of pollution in the environment.

  9. ORGANIC CHELATING REAGENT ON REDOX ADSORPTION OF ACTIVATED CARBON FIBER TOWARDS Au3+

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Organic chelating reagent influences upon the redox adsorption of activated carbon fibertowards Au3- were systematically investigated. The experimental results indicated that the presenceof organic chelating reagent on activated carbon fiber strongly affects adsorption capacity ofactivated carbon fiber towards Au3+. The reduction-adsorption amount of Au3+ increased three timesby the presence of 8-quinolinol. Furthermore, The reduction-adsorption amount of Au3+ depended onthe pH value of adsorption and temperature.

  10. Adsorption of tetracycline from aqueous solutions onto multi-walled carbon nanotubes with different oxygen contents

    OpenAIRE

    Fei Yu; Jie Ma; Sheng Han

    2014-01-01

    Oxidized multi-walled carbon nanotubes (MWCNTs) with different oxygen contents were investigated for the adsorption of tetracycline (TC) from aqueous solutions. As the surface oxygen content of the MWCNTs increased, the maximum adsorption capacity and adsorption coefficient of TC increased to the largest values and then decreased. The relation can be attributed to the interplay between the nanotubes' dispersibility and the water cluster formation upon TC adsorption. The overall adsorption kin...

  11. Substorms on Mercury

    International Nuclear Information System (INIS)

    The Mariner 10 encounter of Mercury provided data showing a strong interaction between the solar wind and the planet similar to a scaled down version of that producing the earth's magnetosphere. Some of the features observed in Mercury's night side magnetosphere suggest time-dependent processes occurring there. Interpreted as temporal events, these features bear striking resemblances to substorm phenomena in the earth's magnetosphere

  12. Mercury's shifting, rolling past

    OpenAIRE

    Trulove, Susan

    2008-01-01

    Patterns of scalloped-edged cliffs or lobate scarps on Mercury's surface are thrust faults that are consistent with the planet shrinking and cooling with time. However, compression occurred in the planet's early history and Mariner 10 images revealed decades ago that lobate scarps are among the youngest features on Mercury. Why don't we find more evidence of older compressive features?

  13. Enhancement of CO2 adsorption on nanoporous chromium terephthalate (MIL-101) by amine modification

    Institute of Scientific and Technical Information of China (English)

    Mansoor Anbia; Vahid Hoseini

    2012-01-01

    Carbon dioxide (CO2) adsorption on a standard metal-organic framework MIL-101 and a pentaethylenehexamine modified MIL-101 (PEHA-MIL-101) are investigated and compared in this study.The adsorbent samples were characterized by XRD,FT-IR and nitrogen adsorption-desorption isotherms analysis.CO2 adsorption capacity was measured by a volumetric method.MIL-101 and PEHA-MIL-101 exhibited CO2 adsorption capacities of 0.85 and 1.3 mmolCO2/gadsorbent at 10 bar and 298 K,respectively.It is observed that CO2 adsorption capacity was fairly improved about 50% after amine modification.

  14. Adsorción de cadmio, cromo y mercurio en suelos del Valle del Cauca a varios valores de pH Cadmium, chromium and mercury adsorption on Cauca Valley soils as a function of pH

    Directory of Open Access Journals (Sweden)

    García O. Álvaro

    1991-12-01

    were collected and prepared for sorption experiments adjusting the pH to 5.7,6.5 and 7.8 values using, 1,4 and 12% acetic acid or 0.01 N NaOH. Six saturating solution of each metal (0.0, 0.28, 0.56, 1.12 and 2.25 mg L-1 were added to 0.25 g air dried and ground to pass a 2-mm sieve soil samples. The soil solution suspensions were shaken for 25 minutes and then extracted with 0.01N HC1. Cadmium; Cr and Hg concentrations were determined by atomic absorption spectrofotometry. The difference between the initial and final metal solution concentration was considered to be soil adsorbed and the amount 0.01 N HC1 extracted as the metal retained by the soil. Cadmium adsorption in all the soils was higher at neutral or alkaline pH values due to the predominance of divalent solubles or insoluble metalanion complexes formed in the soil at pH values higter than 7.0. The Cr and Hg adsorption is higher at acid values of pH due to the formation of complexes with the organic matter (chelation or with Fe, Al or Mn hydrous oxids wich are favoreced at this pH values. The lower 0.01N HC1 extraction (higher retention was observed at pH values 6.4-6.6 in all the soils suggesting that in this range of pH this heavy metals are strongly adsorbed by the exchange complex and are not available to plants.

  15. Adsorption of Chlortetracycline from Water by Rectories

    Institute of Scientific and Technical Information of China (English)

    吕国诚; 吴丽梅; 王晓龙; 廖立兵; 王小雨

    2012-01-01

    The removal of antibiotics from water by clay minerals has become the focus of research due to their strong adsorptive ability. In this study, adsorption of chlortetracycline (CTC) onto rectories was conducted and the effects of time, concentration, temperature and pH were investigated. Experimental results showed that adsorption equilibrium was reached in 8 h. Based on the Langmuir model, the maximum adsorption capacity of CTC on rectories was 177.7 mg·g 1 at room temperature. By the study on adsorption dynamics, it is found that the kinetic date fit the pseudo-second-order model well. The adsorption of CTC by rectories is endothermic and the free energy is in the range of 10 to 30 kJ·mol 1 . The pH value of solution has significant effects on adsorption and the optimal pH is at acidity (pH 2-6). At concentration of 2500 mg·L 1 , the intercalated CTC produces an interlayer space with a height of 1.38 nm, which is 1.12 nm in raw rectories, suggesting that the adsorption occurs between layers of rectories.

  16. Study on copper adsorption on olivine

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The copper adsorption on olivine supplied by A/S Olivine production plant at Aheim in western Norway has been studied. The factors which affect the uptake of copper have been evaluated. The results reveal that the equilibrium pH in aqueous solution has the greatest influence on the copper adsorption thanks to the competitive adsorption between proton and copper ions, and the adsorption of copper to olivine increases rapidly with the pH increasing from 4 to 6. The initial copper concentration and olivine dose also possess significant effect on copper adsorption. The adsorption efficieny of copper increases with the increase of olivine dose or the decrease of initial copper concentration at the same pH. The ionic strength effect on the adsorption has also been investigated, but it owns little effect on the adsorption process of copper due to the formation of inner sphere surface complexation of copper on olivine. The experimental data show that olivine has a high acid buffer capacity and is an effective adsorbent for copper.

  17. Adsorption characteristics of siloxanes in landfill gas by the adsorption equilibrium test.

    Science.gov (United States)

    Nam, Sangchul; Namkoong, Wan; Kang, Jeong-Hee; Park, Jin-Kyu; Lee, Namhoon

    2013-10-01

    Due to the increase in energy cost by constantly high oil prices and the obligation to reduce greenhouse effect gases, landfill gas is frequently used as an alternative energy source for producing heat and electricity. Most of landfill gas utility facilities, however, are experiencing problems controlling siloxanes from landfill gas as their catalytic oxidizers are becoming fouled by silicon dioxide dust. To evaluate adsorption characteristics of siloxanes, an adsorption equilibrium test was conducted and parameters in the Freundlich and Langmuir isotherms were analyzed. Coconut activated carbon (CA1), coal activated carbon (CA2), impregnated activated carbon (CA3), silicagel (NCA1), and activated alumina (NCA2) were used for the adsorption of the mixed siloxane which contained hexamethyldisiloxane (L2), octamethylcyclotetrasiloxane (D4), and decamethylcyclopentasiloxane (D5). L2 had higher removal efficiency in noncarbon adsorbents compared to carbon adsorbents. The application of Langmuir and Freundlich adsorption isotherm demonstrated that coconut based CA1 and CA3 provided higher adsorption capacity on L2. And CA2 and NCA1 provided higher adsorption capacity on D4 and D5. Based on the experimental results, L2, D4, and D5 were converted by adsorption and desorption in noncarbon adsorbents. Adsorption affinity of siloxane is considered to be affect by the pore size distribution of the adsorbents and by the molecular size of each siloxane. PMID:23684695

  18. Getting Mercury out of Schools.

    Science.gov (United States)

    1999

    This guide was prepared while working with many Massachusetts schools to remove items that contain mercury and to find suitable alternatives. It contains fact sheets on: mercury in science laboratories and classrooms, mercury in school buildings and maintenance areas, mercury in the medical office and in medical technology classrooms in vocational…

  19. Municipal actions to reduce mercury

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2005-03-15

    This paper presented proper management practices for products containing mercury. The measures can help reduce mercury releases, occupational exposure and mercury spills, thereby preventing impacts on human health and the environment. Despite mercury's toxic nature, many common products that contain mercury are commercially available. These include thermostats, thermometers, fluorescent lamps, pressure measuring devices, electrical switches and relays, and dental amalgam. Mercury emissions are also associated with base metal smelting, waste incineration and coal-fired power generation. Mercury in the environment is a global issue, because it can travel in the atmosphere on wind currents. The actions taken by municipalities to address the issue include reducing or eliminating mercury releases from internal municipal operations and sources within the community. This document provided guidance on how to develop a Municipal Mercury Elimination Policy and Plan that will help reduce mercury releases. It presented information and case studies that will help municipalities manage mercury-containing products found in municipal buildings and street lighting. Information on sources of mercury from within the community was presented along with case studies that can help municipalities determine where community action is needed to reduce mercury releases. The 5 modules of this document were intended to help municipalities identify priorities, timelines and budget requirements for mercury initiatives. It was emphasized that municipalities that adopt a Municipal Mercury Elimination Policy and Plan formally commit to reducing and eliminating mercury from the environment. tabs., figs.

  20. Adsorption and wetting.

    OpenAIRE

    Schlangen, L.J.M.

    1995-01-01

    Adsorption and wetting are related phenomena. In order to improve knowledge of both and their relations, experiments, thermodynamics and a theoretical interpretation have been connected, starring n-alkanes.Starting from the Gibbs adsorption equation thermodynamic relations between vapour adsorption and wetting are derived. The surface pressure of a film, formed by vapour adsorption on a solid surface, is calculated by integrating the vapour adsorption isotherm. The surface pressure at the sat...

  1. Fibrous polymer-grafted chitosan/clay composite beads as a carrier for immobilization of papain and its usability for mercury elimination.

    Science.gov (United States)

    Metin, Ayşegül Ülkü; Alver, Erol

    2016-07-01

    Papain, which is an industrially important enzyme, has been immobilized on fibrous polymer-modified composite beads, namely poly(methacrylic acid)-grafted chitosan/clay. Characterization studies have been done using FTIR and SEM analysis. Operating parameters such as pH and initial concentration of papain have been varied to obtain the finest papain immobilized polymer-modified composite beads. The immobilization capacity of composite beads has been determined as 34.47 ± 1.18 (n = 3) mg/g. The proteolytic activity of immobilized papain was operated using bovine serum albumin (BSA) and maximum velocity (V max) and Michaelis-Menten constant (Km) values of the free and immobilized enzymes were determined using Lineweaver-Burk and Eadie-Hofstee equations. Usability of papain immobilized polymer-modified composite beads as adsorbents for the elimination of mercury was investigated. The maximum removal capacity of PIPMC beads has been found to be 4.88 ± 0.21 mg Hg/g when the initial metal concentration and weight of polymer-modified composite beads were 50 mg/L and 0.04 g at pH 7, respectively. Mercury removal performance of the papain immobilized polymer-modified composite beads was investigated in conjunction with Cu (II), Zn (II) and Cd (II) ions. The mercury adsorption capacity of papain immobilized polymer-modified composite beads was a slight reduction from 1.15 to 0.89 mg/g in presence of multiple metal salts. PMID:27013506

  2. Fibrous polymer-grafted chitosan/clay composite beads as a carrier for immobilization of papain and its usability for mercury elimination.

    Science.gov (United States)

    Metin, Ayşegül Ülkü; Alver, Erol

    2016-07-01

    Papain, which is an industrially important enzyme, has been immobilized on fibrous polymer-modified composite beads, namely poly(methacrylic acid)-grafted chitosan/clay. Characterization studies have been done using FTIR and SEM analysis. Operating parameters such as pH and initial concentration of papain have been varied to obtain the finest papain immobilized polymer-modified composite beads. The immobilization capacity of composite beads has been determined as 34.47 ± 1.18 (n = 3) mg/g. The proteolytic activity of immobilized papain was operated using bovine serum albumin (BSA) and maximum velocity (V max) and Michaelis-Menten constant (Km) values of the free and immobilized enzymes were determined using Lineweaver-Burk and Eadie-Hofstee equations. Usability of papain immobilized polymer-modified composite beads as adsorbents for the elimination of mercury was investigated. The maximum removal capacity of PIPMC beads has been found to be 4.88 ± 0.21 mg Hg/g when the initial metal concentration and weight of polymer-modified composite beads were 50 mg/L and 0.04 g at pH 7, respectively. Mercury removal performance of the papain immobilized polymer-modified composite beads was investigated in conjunction with Cu (II), Zn (II) and Cd (II) ions. The mercury adsorption capacity of papain immobilized polymer-modified composite beads was a slight reduction from 1.15 to 0.89 mg/g in presence of multiple metal salts.

  3. Comparative research on removing mercury by powder activated carbon on bag filter%纯活性炭粉末布袋脱汞的比较研究

    Institute of Scientific and Technical Information of China (English)

    陈振松; 杨国华; 黄三; 于建伟; 盛伟鹏; 谭均军

    2011-01-01

    For improving mercury removal efficiency of activated carbon(AC) injection upstream a bag filter and the utilization ratio of powder activated carbon(PAC), mercury removal experiments were conducted in a small-scale bag filter with pure PAC as the sorbent. The results indicate that the average mercury removal efficiency(AMRE) was 99.1% within 85 minutes for the first adsorption, and the adsorption time was 1335 minutes with removal efficiency above 75%. For comparison, other experiments were conducted using PAC mixed with different pro- portion of fly ash. The results show that the AMRE within 85 minutes for the first adsorption was only 19.3% and the removal efficiency fell to 0 after 165 minutes with fly ash as the sot- bent. The AMRE within 85 minutes for the first adsorption were 99.1~,95%, 85.3%, 79.7%, and 59.6%, and the mercury adsorption capacity with removal efficiency above 75% were 196.1 172.5, 133.8, 123.6, and 21.7 μg Hg/g AC for the PAC based sorbents mixed with the fly ash of 0, 20%, 50%, 80%, and95%, respectively. Hence, the mercury removal new technology by pure PAC on bag filter has better mercury removal efficiency and utilization ratio of PAC.%为解决布袋除尘器活性炭(AC)喷射脱汞传统技术中活性炭粉末利用率低、脱汞效率低的问题,提出了纯活性炭粉末一布袋脱汞新技术,采用纯活性炭粉末为吸附剂,进行了布袋脱汞实验研究,结果表明:纯活性炭粉末初次吸附的前85min的平均脱汞效率为99.1%,脱汞效率大于75%的累计吸附时间为1335min.为便于比较,进行了活性炭粉末掺杂不同比例飞灰的脱汞实验,结果表明:纯飞灰在初次吸附的前85min脱汞效率仅为19.3%,165min时脱汞效率已经下降为0.活性炭粉末掺杂飞灰比例分别为0,20%,50%,80%,95%时,初次吸附的前85min的平均脱汞效率分别为99.1%,95%,85.3%,79.7%,59.6%,每

  4. Adsorption characteristics of zinc ions on sodium dodecyl sulfate in process of micellar-enhanced ultrafiltration

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    To separate zinc ions from aqueous solution efficiently, micellar-enhanced ultrafiltration(MEUF) of hollow ultrafiltration membrane was used with sodium dodecyl sulfate(SDS) as surfactant. The formation of micellar and the adsorption mechanism were investigated, including the influence of the ratio of SDS to zinc ions on the micelle quantity, the micelle ratio, the gross adsorptive capacity, the rejection of zinc ions and the adsorption isotherm law. The results show that the rejection rate of zinc ions reaches 97% and the adsorption of zinc ions on SDS conforms to the Langmuir adsorption isotherm and the adsorption is a chemical adsorption process.

  5. Demonstration of Mer-Cure Technology for Enhanced Mercury Control

    Energy Technology Data Exchange (ETDEWEB)

    John Marion; Dave O' Neill; Kevin Taugher; Shin Kang; Mark Johnson; Gerald Pargac; Jane Luedecke; Randy Gardiner; Mike Silvertooth; Jim Hicks; Carl Edberg; Ray Cournoyer; Stanley Bohdanowicz; Ken Peterson; Kurt Johnson; Steve Benson; Richard Schulz; Don McCollor; Mike Wuitshick

    2008-06-01

    Alstom Power Inc. has completed a DOE/NETL-sponsored program (under DOE Cooperative Agreement No. De-FC26-07NT42776) to demonstrate Mer-Cure{trademark}, one of Alstom's mercury control technologies for coal-fired boilers. The Mer-Cure{trademark}system utilizes a small amount of Mer-Clean{trademark} sorbent that is injected into the flue gas stream for oxidation and adsorption of gaseous mercury. Mer-Clean{trademark} sorbents are carbon-based and prepared with chemical additives that promote oxidation and capture of mercury. The Mer-Cure{trademark} system is unique in that the sorbent is injected into an environment where the mercury capture kinetics is accelerated. The full-scale demonstration program originally included test campaigns at two host sites: LCRA's 480-MW{sub e} Fayette Unit No.3 and Reliant Energy's 190-MW{sub e} Shawville Unit No.3. The only demonstration tests actually done were the short-term tests at LCRA due to budget constraints. This report gives a summary of the demonstration testing at Fayette Unit No.3. The goals for this Mercury Round 3 program, established by DOE/NETL under the original solicitation, were to reduce the uncontrolled mercury emissions by 90% at a cost significantly less than 50% of the previous target of $60,000/lb mercury removed. The results indicated that Mer-Cure{trademark} technology could achieve mercury removal of 90% based on uncontrolled stack emissions. The estimated costs for 90% mercury control, at a sorbent cost of $0.75 to $2.00/lb respectively, were $13,400 to $18,700/lb Hg removed. In summary, the results from demonstration testing show that the goals established by DOE/NETL were met during this test program. The goal of 90% mercury reduction was achieved. Estimated mercury removal costs were 69-78% lower than the benchmark of $60,000/lb mercury removed, significantly less than 50% of the baseline removal cost.

  6. Development of mercury control technology for coal-fired systems

    Energy Technology Data Exchange (ETDEWEB)

    Livengood, D.C.; Huang, H.S.; Mendelsohn, M.H.; Wu, Jiann M.

    1995-08-01

    The emission of hazardous air pollutants (air toxics) from various industrial processes has emerged as a major environmental issue that was singled out for particular attention in the Clean Air Act Amendments of 1990. In particular, mercury emissions are the subject of several current EPA studies because of concerns over possible serious effects on human health. Some of those emissions originate in the combustion of coal, which contains trace amounts of mercury, and are likely to be the subject of control requirements in the relatively near future. Data collected by the Department of Energy (DOE) and the Electric Power Research Institute (EPRI) at operating electric-power plants have shown that conventional flue-gas cleanup (FGC) technologies are not very effective in controlling emissions of mercury in general, and are particularly poor at controlling emissions of elemental mercury. This paper gives an overview of research being conducted at Argonne National Laboratory on improving the capture of mercury in flue gas through the use of dry sorbents and/or wet scrubbers. The results and conclusions to date from the Argonne research on dry sorbents can be summarized as follows: lime hydrates, either regular or high-surface-area, are not effective in removing elemental mercury; mercury removals are enhanced by the addition of activated carbon; mercury removals with activated carbon decrease with increasing temperature, larger particle size, and decreasing mercury concentration in the gas; chemical pretreatment (e.g., with sulfur or CaCl{sub 2}) can greatly increase the removal capacity of activated carbon; chemically treated mineral substrates have the potential to be developed into effective and economical mercury sorbents; sorbents treated with different chemicals respond in significantly different ways to changes in flue-gas temperature.

  7. Detoxification of mercury pollutant leached from spent fluorescent lamps using bacterial strains.

    Science.gov (United States)

    Al-Ghouti, Mohammad A; Abuqaoud, Reem H; Abu-Dieyeh, Mohammed H

    2016-03-01

    The spent fluorescent lamps (SFLs) are being classified as a hazardous waste due to having mercury as one of its main components. Mercury is considered the second most toxic heavy metal (arsenic is the first) with harmful effects on animal nervous system as it causes different neurological disorders. In this research, the mercury from phosphor powder was leached, then bioremediated using bacterial strains isolated from Qatari environment. Leaching of mercury was carried out with nitric and hydrochloric acid solutions using two approaches: leaching at ambient conditions and microwave-assisted leaching. The results obtained from this research showed that microwave-assisted leaching method was significantly better in leaching mercury than the acid leaching where the mercury leaching efficiency reached 76.4%. For mercury bio-uptake, twenty bacterial strains (previously isolated and purified from petroleum oil contaminated soils) were sub-cultured on Luria Bertani (LB) plates with mercury chloride to check the bacterial tolerance to mercury. Seven of these twenty strains showed a degree of tolerance to mercury. The bio-uptake capacities of the promising strains were investigated using the mercury leached from the fluorescent lamps. Three of the strains (Enterobacter helveticus, Citrobacter amalonaticus, and Cronobacter muytjensii) showed bio-uptake efficiency ranged from 28.8% to 63.6%. PMID:26725036

  8. Installation of the Ferranti Mercury computer in building 2 on 30 June 1958

    CERN Multimedia

    1958-01-01

    The Ferranti Mercury was CERN's first "central" computer. It was installed in building 2 on 30 June 1958. The Mercury's performance did not compare to the simplest of today's pocket calculators. Its clock speed was a modest 1 MHz and its RAM capacity was 2000 20-bit words.

  9. Poultry manure as raw material for mercury adsorbents in gas applications

    Energy Technology Data Exchange (ETDEWEB)

    Klasson, K.T.; Lima, I.M.; Boihem, L.L. [USDA ARS, New Orleans, LA (United States)

    2009-09-30

    The quantity of poultry manure generated each year is large, and technologies that take advantage of the material should be explored. At the same time, increased emphasis on the reduction of mercury emissions from coal-fired electric power plants has resulted in environmental regulations that may, in the future, require application of activated carbons as mercury sorbents. The sorbents could be injected into the flue gas stream, where they could adsorb the mercury. The sorbents (now containing mercury) would be removed via filtration or other means from the flue gas. Our preliminary work has demonstrated that activated carbon made from poultry manure can adsorb mercury from air with good efficiency. In laboratory experiments, an activated carbon made from turkey cake manure removed the majority of elemental mercury from a hot air stream. Other activated carbons made from chicken and turkey litter manure were also efficient. In general, unwashed activated carbons made from poultry manure were more efficient in removing mercury than their acid-washed counterparts. The results suggest that the adsorption of mercury was mainly due to chemisorption on the surface of the carbon. Other potential uses for the activated carbons are the removal of mercury from air and natural gas.

  10. Batch and continuous adsorption of strontium by plant root tissues

    Energy Technology Data Exchange (ETDEWEB)

    Jyhping Chen [Chang Gung Coll. of Medicience and Technology, Taoyuan, Taiwan (China). Dept. of Chemical Engineering

    1997-06-01

    Strontium (Sr) ions in aqueous solutions could be adsorbed by root tissue powders of Amaranthus spinosus, a common weed found in the fields. The adsorption isotherm could be fitted by either the Langmuir or the Freundlich model with the maximum adsorption capacity being 12.89 mg/g from the Langmuir isotherm. The maximum adsorption capacity of the biosorbent decreased with increasing temperature, whereas alkaline pretreatment enhanced the adsorption capacity 1.9 fold. Alginate gel beads (1 mm diameter) containing the root tissue powders were prepared and packed in a column for continuous adsorption/desorption of Sr in solution. Efficient desorption of Sr could be carried out with 0.1 M CaCl{sub 2} to give a concentrated Sr solution with 94% recovery. (author).

  11. Batch and continuous adsorption of strontium by plant root tissues

    International Nuclear Information System (INIS)

    Strontium (Sr) ions in aqueous solutions could be adsorbed by root tissue powders of Amaranthus spinosus, a common weed found in the fields. The adsorption isotherm could be fitted by either the Langmuir or the Freundlich model with the maximum adsorption capacity being 12.89 mg/g from the Langmuir isotherm. The maximum adsorption capacity of the biosorbent decreased with increasing temperature, whereas alkaline pretreatment enhanced the adsorption capacity 1.9 fold. Alginate gel beads (1 mm diameter) containing the root tissue powders were prepared and packed in a column for continuous adsorption/desorption of Sr in solution. Efficient desorption of Sr could be carried out with 0.1 M CaCl2 to give a concentrated Sr solution with 94% recovery. (author)

  12. A comparison of three adsorption equations and sensitivity study of parameter uncertainty effects on adsorption refrigeration thermal performance estimation

    Science.gov (United States)

    Zhao, Yongling; Hu, Eric; Blazewicz, Antoni

    2012-02-01

    This paper presents isosteric-based adsorption equilibrium tests of three activated carbon samples with methanol as an adsorbate. Experimental data was fitted into Langmuir equation, Freundlich equation and Dubinin-Astakov (D-A) equation, respectively. The fitted adsorption equations were compared in terms of agreement with experimental data. Moreover, equation format's impacts on calculation of the coefficient of performance (COP) and refrigeration capacity of an adsorption refrigeration system was analyzed. In addition, the sensitivity of each parameter in each adsorption equation format to the estimation of cycle's COP and refrigeration capacity was investigated. It was found that the D-A equation is the best form for presenting the adsorptive property of a carbon-methanol working pair. The D-A equation is recommended for estimating thermal performance of an adsorption refrigeration system because simulation results obtained using the D-A equation are less sensitive to errors of experimentally determined D-A equation's parameters.

  13. Mercury Pollution Control Technology of Mercury Containing Equipment%含汞设备汞污染控制技术

    Institute of Scientific and Technical Information of China (English)

    牛瑞; 蒋洪; 陈倩

    2016-01-01

    Mercury pollutants in natural gas not only cause pollution and corrosion of equip-ment, the impact of production efficiency, but also on the human body and the environ-ment there is a definite harm. Equipment of mercury exists mainly in the form of elemental mercury, particle size, adsorption and permeation on the inner wall of the equipment, or with the oil, furring together adhesion on the inner wall. Mercury will cause corrosion to equipment, especially for aluminum equipment. This paper summarizes the general methods of domestic and foreign experience and metal cleaning,proposed containing mercury remov-al methods including artificial jet cleaning method,the steam cleaning method,cyclic chem-ical cleaning method. According to the device type and mercury pollution degree, choose suitable mercury cleaning method, and puts forward equipment for mercury technical re-quirements, of containing mercury pollution control, Recommended when mercury envi-ronment homework allows contact concentration (the PEL) for 20 μg/m3. At run time, mercury containing equipment should be timely detection and cleaning,in order to avoid the harm from mercury.%天然气中的汞不仅对设备造成污染和腐蚀,而且对人体及环境都有一定的危害。设备内的汞主要以单质汞的形式存在,颗粒大小不一,吸附渗透在设备内壁或与油污、水垢等一起黏附在内壁上。汞会对设备造成腐蚀,尤其是铝制设备。归纳并综合国内外经验和金属清洗的一般方法,提出了含汞设备的汞清除方法,包括人工喷射清洗法、蒸汽清洗法、循环化学清洗法等,根据设备类型和汞污染程度选择合适的清汞方法;提出了设备清汞的技术要求,推荐含汞环境作业时的允许接触浓度(PEL)为20μg/m3。含汞设备在运行时应及时检测汞含量,定期清汞,以避免汞带来的危害。

  14. Total mercury content in fish und molluscs from Adriatic sea

    International Nuclear Information System (INIS)

    In regard to a long known and still persisting problem of the ecosystem loaded with mercury, total mercury contents in different species of fish and molluscs in the Adriatic Sea have been followed in an interval of 12 years. Total mercury concentrations were determined by cold vapour atomic adsorption spectrometry (CVAAS) at 253. 7 nm after digestion of the edible of fish tissues. The results of analysis reveal positive shifts and unlike the samples in a previous study all the investigated samples meet the conditions of the Public Health Regulations on the quantity of pesticides, mycotoxins, metals, histamine and similar substances that may occur in foodstuff and on other conditions as to the standards of foodstuff and objects of general use, which fixed the total Hg content at maximum of 0.5 mg/kg on the basis of fresh mass. (orig.)

  15. Catalysts for oxidation of mercury in flue gas

    Science.gov (United States)

    Granite, Evan J.; Pennline, Henry W.

    2010-08-17

    Two new classes of catalysts for the removal of heavy metal contaminants, especially mercury (Hg) from effluent gases. Both of these classes of catalysts are excellent absorbers of HCl and Cl.sub.2 present in effluent gases. This adsorption of oxidizing agents aids in the oxidation of heavy metal contaminants. The catalysts remove mercury by oxidizing the Hg into mercury (II) moieties. For one class of catalysts, the active component is selected from the group consisting of iridium (Ir) and iridum-platinum (Ir/Pt) alloys. The Ir and Ir/Pt alloy catalysts are especially corrosion resistant. For the other class of catalyst, the active component is partially combusted coal or "Thief" carbon impregnated with Cl.sub.2. Untreated Thief carbon catalyst can be self-activating in the presence of effluent gas streams. The Thief carbon catalyst is disposable by means of capture from the effluent gas stream in a particulate collection device (PCD).

  16. Total mercury content in fish und molluscs from Adriatic sea

    Energy Technology Data Exchange (ETDEWEB)

    Vedrina-Dragojevic, I. [Zagreb Univ. (Croatia). Dept. of Food Chemistry; Dragojevic, D. [Water Quality Dept., Waterworks, Zagreb (Croatia); Bujan, M. [Zagreb Univ. (Croatia). Dept. of Chemistry

    2002-07-01

    In regard to a long known and still persisting problem of the ecosystem loaded with mercury, total mercury contents in different species of fish and molluscs in the Adriatic Sea have been followed in an interval of 12 years. Total mercury concentrations were determined by cold vapour atomic adsorption spectrometry (CVAAS) at 253. 7 nm after digestion of the edible of fish tissues. The results of analysis reveal positive shifts and unlike the samples in a previous study all the investigated samples meet the conditions of the Public Health Regulations on the quantity of pesticides, mycotoxins, metals, histamine and similar substances that may occur in foodstuff and on other conditions as to the standards of foodstuff and objects of general use, which fixed the total Hg content at maximum of 0.5 mg/kg on the basis of fresh mass. (orig.)

  17. Enantiomeric Selective Adsorption of Amino Acid by Polysaccharide Composite Materials

    OpenAIRE

    Duri, Simon; Tran, Chieu D.

    2014-01-01

    A composite containing cellulose (CEL) and chitosan (CS) synthesized by a simple and recyclable method by using butylmethylimmidazolium chloride, an ionic liquid, was found to exhibit remarkable enantiomeric selectivity toward adsorption of amino acids. 100%CS shows the highest adsorption capacity and enantiomeric selectivity. A racemic amino acid can be enantiomerically resolved by 100%CS in about 96–120 hrs. Interestingly, adsorption by 50:50 CEL:CS is more similar to that by 100%CS than to...

  18. Mercury's Protoplanetary Mass

    CERN Document Server

    Herndon, J M

    2004-01-01

    Major element fractionation among chondrites has been discussed for decades as ratios relative to Si or Mg. Recently, by expressing ratios relative to Fe, I discovered a new relationship admitting the possibility that ordinary chondrite meteorites are derived from two components, a relatively oxidized and undifferentiated, primitive component and a somewhat differentiated, planetary component, with oxidation state like the highly reduced enstatite chondrites, which I suggested was identical to Mercury's complement of lost elements. Here, on the basis of that relationship, I derive expressions, as a function of the mass of planet Mercury and the mass of its core, to estimate the mass of Mercury's lost elements, the mass of Mercury's alloy and rock protoplanetary core, and the mass of Mercury's gaseous protoplanet. Although Mercury's mass is well known, its core mass is not, being widely believed to be in the range of 70-80 percent of the planet mass. For a core mass of 75 percent, the mass of Mercury's lost el...

  19. Mercury's Dynamic Magnetic Tail

    Science.gov (United States)

    Slavin, James A.

    2010-01-01

    The Mariner 10 and MESSENGER flybys of Mercury have revealed a magnetosphere that is likely the most responsive to upstream interplanetary conditions of any in the solar system. The source of the great dynamic variability observed during these brief passages is due to Mercury's proximity to the Sun and the inverse proportionality between reconnection rate and solar wind Alfven Mach number. However, this planet's lack of an ionosphere and its small physical dimensions also contribute to Mercury's very brief Dungey cycle, approx. 2 min, which governs the time scale for internal plasma circulation. Current observations and understanding of the structure and dynamics of Mercury's magnetotail are summarized and discussed. Special emphasis will be placed upon such questions as: 1) How much access does the solar wind have to this small magnetosphere as a function of upstream conditions? 2) What roles do heavy planetary ions play? 3) Do Earth-like substorms take place at Mercury? 4) How does Mercury's tail respond to extreme solar wind events such coronal mass ejections? Prospects for progress due to advances in the global magnetohydrodynamic and hybrid simulation modeling and the measurements to be taken by MESSENGER after it enters Mercury orbit on March 18, 2011 will be discussed.

  20. Adsorption performances and refrigeration application of adsorption working pair of CaCl2-NH3

    Institute of Scientific and Technical Information of China (English)

    WANG; Liwei; WANG; Ruzhu; WU; Jingyi; WANG; Kai

    2004-01-01

    The adsorption performance of CaCl2-NH3 is studied under the condition of different expansion spaces for adsorbent, andthe relationships between adsorption performance of CaCl2-NH3 and the phenomena of swelling and agglomeration during adsorption are researched. It is found that the performance stability is related to the ratio of expansion space to the volume of adsorbent ras, and the performance attenuation is serious in the case of large ras. Severe adsorption hysteresis exists in the process of adsorption and desorption at the same evaporating and condensing temperatures, which is related to the stability constant of chemical reaction. This phenomenon cannot be explained by the theory of physical adsorption. Moderate agglomeration will be beneficial to the formation of ammoniate complex; the magnitude of expansion space will affect adsorption performance. Analysis shows that the activated energy needed in the process of adsorption for the sample with ras of 2:1 is less than that for the sample with ras of 3:1.The refrigeration performance of CaCl2-NH3 is predicted from experiments. The cooling capacity of one adsorption cycle is about 945.4 kJ/kg for the adsorbent with an ras of 2:1 at the evaporating temperature of 0℃.

  1. New insight into the biological treatment by activated sludge: the role of adsorption process.

    Science.gov (United States)

    Zhang, Xiaochun; Li, Xinrun; Zhang, Qingrui; Peng, Qiuming; Zhang, Wen; Gao, Faming

    2014-02-01

    The objective of this study was to evaluate the effect of adsorption on the biological treatment process of wastewater. In the absence of substrate in the water, activated sludge developed well in the first hour, indicating that the growth of microorganism was not directly related to substrate concentration and the dissolved organic matter in the water assays were performed, no organic matter was detected out, revealing that there was no desorption in the activated sludge adsorption process. Activated sludge batch growth experiments in the presence of different adsorption capacities indicated that specific growth rate increased as specific adsorption capacity increased. The experiment on the relationship of adsorption capacity and substrate concentration or sludge concentration was also carried out. Specific adsorption capacity increased as sludge load increased, presenting linear correlation. The experiment results showed that adsorption should be taken into account in the study of the biological treatment process of wastewater.

  2. Preparation of Aminated Macroporous Polyvinyl Alcohol Resins and Evaluation for Bilirubin Adsorption

    Institute of Scientific and Technical Information of China (English)

    WANG Wei-chao; ZHANG Sheng-nan; HU Yue-han; XIE Hui; OU Lai-liang; YU Yao-ting; KONG De-ling; GU Han-qing

    2008-01-01

    In the present study we prepared macroporous polyvinyl alcohol beads. A series of bilirubin adsorbents were generated by immobilization of eight amine agents to the beads as ligands. The adsorption of bilirubin was evaluated by in vitro static and dynamic adsorption tests. The results show that these adsorbents have excellent adsorption efficiency and capacity. Among the eight ligands, trimethylamine (TMA), triethylamine (TEA) and 1,6- hexanediamine(HAD) showed the highest adsorption capacity. The adsorption equilibrium can be achieved in half an hour, and the adsorption percentage of bilirubin was up to 80%. Static electricity and hydrophobic interaction played the main role in bilirubin adsorption, and the adsorption was found to match the monolayer model. The excellent adsorption of these adsorbents indicates their potential in clinical treatment.

  3. Equilibrium, kinetic and thermodynamic studies on the adsorption of phenol onto graphene

    Energy Technology Data Exchange (ETDEWEB)

    Li, Yanhui, E-mail: liyanhui@tsinghua.org.cn [Laboratory of Fiber Materials and Modern Textile, The Growing Base for State Key Laboratory, College of Electromechanical Engineering, Qingdao University, 308 Ningxia Road, Qingdao 266071 (China); Du, Qiuju; Liu, Tonghao; Sun, Jiankun; Jiao, Yuqin [Laboratory of Fiber Materials and Modern Textile, The Growing Base for State Key Laboratory, College of Electromechanical Engineering, Qingdao University, 308 Ningxia Road, Qingdao 266071 (China); Xia, Yanzhi, E-mail: xiayzh@qdu.edu.cn [Laboratory of Fiber Materials and Modern Textile, The Growing Base for State Key Laboratory, College of Electromechanical Engineering, Qingdao University, 308 Ningxia Road, Qingdao 266071 (China); Xia, Linhua; Wang, Zonghua [Laboratory of Fiber Materials and Modern Textile, The Growing Base for State Key Laboratory, College of Electromechanical Engineering, Qingdao University, 308 Ningxia Road, Qingdao 266071 (China); Zhang, Wei; Wang, Kunlin; Zhu, Hongwei; Wu, Dehai [Key Laboratory for Advanced Manufacturing by Material Processing Technology, Department of Mechanical Engineering, Tsinghua University, Beijing 100084 (China)

    2012-08-15

    Graphical abstract: The effect of temperature on phenol adsorbed by graphene shows that the equilibrium adsorption capacity of phenol increases with the increase in temperature from 285 to 333 K. Increasing adsorption capacities with temperature indicates that the adsorption of phenol is controlled by an endothermic reaction. Highlights: ► The graphene has high phenol adsorption capacity. ► The graphene has a high specific surface area of 305 m{sup 2}/g. ► The adsorption capacity is high at acidic pH range. ► The graphene has rapid phenol adsorption rate. ► Phenol adsorption is a spontaneous and endothermic process. -- Abstract: Graphene, a new member of carbon family, has been prepared, characterized and used as adsorbent to remove phenol from aqueous solution. The effect parameters including pH, dosage, contact time, and temperature on the adsorption properties of phenol onto graphene were investigated. The results showed that the maximum adsorption capacity can reach 28.26 mg/g at the conditions of initial phenol concentration of 50 mg/L, pH 6.3 and 285 K. Adsorption data were well described by both Freundlich and Langmuir models. The kinetic study illustrated that the adsorption of phenol onto graphene fit the pseudo second-order model. The thermodynamic parameters indicated that the adsorption of phenol onto graphene was endothermic and spontaneous.

  4. HYDROGEN SULFIDE ADSORPTION BY ALKALINE IMPREGNATED COCONUT SHELL ACTIVATED CARBON

    Directory of Open Access Journals (Sweden)

    HUI SUN CHOO

    2013-12-01

    Full Text Available Biogas is one type of renewable energy which can be burnt to produce heat and electricity. However, it cannot be burnt directly due to the presence of hydrogen sulfide (H2S which is highly corrosive to gas engine. In this study, coconut shell activated carbon (CSAC was applied as a porous adsorbent for H2S removal. The effect of amount of activated carbon and flow rate of gas stream toward adsorption capacity were investigated. Then, the activated carbons were impregnated by three types of alkaline (NaOH, KOH and K2CO3 with various ratios. The effects of various types of alkaline and their impregnation ratio towards adsorption capacity were analysed. In addition, H2S influent concentration and the reaction temperature on H2S adsorption were also investigated. The result indicated that adsorption capacity increases with the amount of activated carbon and decreases with flow rate of gas stream. Alkaline impregnated activated carbons had better performance than unimpregnated activated carbon. Among all impregnated activated carbons, activated carbon impregnated by K2CO3 with ratio 2.0 gave the highest adsorption capacity. Its adsorption capacity was 25 times higher than unimpregnated activated carbon. The result also indicated that the adsorption capacity of impregnated activated carbon decreased with the increment of H2S influent concentration. Optimum temperature for H2S adsorption was found to be 50˚C. In this study, the adsorption of H2S on K2CO3 impregnated activated carbon was fitted to the Langmuir isotherm. The fresh and spent K2CO3 impregnated activated carbon were characterized to study the adsorption process.

  5. Carrying Capacity

    DEFF Research Database (Denmark)

    Schroll, Henning; Andersen, Jan; Kjærgård, Bente

    2012-01-01

    carrying capacity (SCC) and assimilative carrying capacity (ACC). The act mandates that the latter two aspects must be taken into consideration in the local spatial plans. The present study aimed at developing a background for a national guideline for carrying capacity in Indonesian provinces and districts...... carrying capacity (ACC). The act mandates that the latter two aspects must be taken into consideration in the local spatial plans. The present study aimed at developing a background for a national guideline for carrying capacity in Indonesian provinces and districts/cities. Four different sectors (water...

  6. Mercury speciation and its emissions from a 220 MW pulverized coal-fired boiler power plant in flue gas

    Energy Technology Data Exchange (ETDEWEB)

    Yang, X.H.; Zhuo, Y.Q.; Duan, Y.F.; Chen, L.; Yang, L.G.; Zhang, L.A.; Jiang, Y.M.; Xu, X.C. [Southeast University, Nanjing (China). Thermoenergy Engineering Research Institute

    2007-07-15

    Distributions of mercury speciation of Hg{sup 0}, Hg{sup 2+} and Hg{sup P} in flue gas and fly ash were sampled by using the Ontario Hydro Method in a 220 MW pulverized coal-fired boiler power plant in China. The mercury speciation was varied greatly when flue gas going through the electrostatic precipitator (ESP). The mercury adsorbed on fly ashes was found strongly dependent on unburnt carbon content in fly ash and slightly on the particle sizes, which implies that the physical and chemical features of some elemental substances enriched to fly ash surface also have a non-ignored effect on the mercury adsorption. The concentration of chlorine in coal, oxygen and NOx in flue gas has a positive correlation with the formation of the oxidized mercury, but the sulfur in coal has a positive influence on the formation of elemental mercury.

  7. Adsorption of catechol from aqueous solution by aminated hypercrosslinked polymers

    Institute of Scientific and Technical Information of China (English)

    SUN Yue; LI Xiao-tao; XU Chao; CHEN Jin-long; LI Ai-min; ZHANG Quan-xing

    2005-01-01

    Adsorption of catechol from aqueous solution with the hypercrosslinked polymeric adsorbent NDA-100 and its derivatives AH-1,AH-2 and AH-3 aminated by dimethylamine, the commercial resin Amberlite XAD-4 and weakly basic anion exchanger resin D301 was compared. It was found that the aminated hypercrosslinked resins had the highest adsorption capacities among the tested polymers. The empirical Freundlich equation was successfully employed to describe the adsorption process. Specific surface area and micropore structure of the adsorbent, in company with tertiary amino groups on matrix affected the adsorption performance towards catechol. In addition,thermodynamic study was carried out to interpret the adsorption mechanism. Kinetic study testified that the tertiary amino groups on the polymer matrix could decrease the adsorption rate and increase the adsorption apparent activation energy.

  8. Adsorption of Anionic Dyes onto Chitosan-modified Diatomite

    Institute of Scientific and Technical Information of China (English)

    ZHANG Ge-shan; XUE Hong-hai; TANG Xiao-jian; PENG Fei; KANG Chun-li

    2011-01-01

    The purpose of this work is to study the possibility of anionic dyes Reactive Red M-8B(RR)and Direct Green B(DG)adsorbed on chitosan-modified diatomite.The characteristics of adsorbent,adsorption isotherms and the influence of adsorption time,temperature and pH were researched in this work.The results show that the modified diatomite had a much better adsorption capability than the natural diatomite.The adsorption capacities of chitosan-modified diatomite for RR and DG were 94.46 and 137.0 mg/g,respectively.Both adsorption time and adsorption temperature provided a positive effect on the dye adsorption.Within the experimental pH range,the adsorbance was enhanced at lower pH but reduced sharply at high pH.On the basis of the experimental results and discussion,electrostatic attraction is considered as the main mechanism of this chemisorption.

  9. EFFECT OF GAC CHARACTERISTICS ON ADSORPTION OF ORGANIC POLLUTANTS

    Science.gov (United States)

    The impact of the characteristics of granular activated carbon (GAC) on adsorption capacity and on the potential for polymerization of phenolic compounds on the surface of GAC in the presence of molecular oxygen is evaluated in this study. Adsorption isotherm data were collected...

  10. Enhanced sorption of mercury from compact fluorescent bulbs and contaminated water streams using functionalized multiwalled carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Gupta, Avinash; Vidyarthi, S.R. [Department of Chemical Engineering Harcourt Butler Technological Institute, Kanpur 208001, U.P. (India); Sankararamakrishnan, Nalini, E-mail: nalini@iitk.ac.in [Centre for Environmental Science and Engineering Indian Institute of Technology Kanpur, Kanpur 208016, U.P. (India)

    2014-06-01

    Highlights: • Oxidized (CNT-OX), CNT-I, CNT-S were prepared. • Capacity of CNT-S (151.5 mg/g) was higher than other CNTs. • Applied to the removal of Hg(II) from spiked and natural coal wash waters. • Applied to the removal of Hg(0) from compact fluorescent lamps. - Abstract: Three different functionalized multiwalled carbon nanotubes were prepared, namely, oxidized CNTs (CNT-OX), iodide incorporated MWCNT (CNT-I) and sulfur incorporated MWCNT (CNT-S). The as prepared adsorbents were structurally characterized by various spectral techniques like scanning electron microscopy (SEM), energy dispersive X-ray (EDAX), Brunauer, Emmett, and Teller (BET) surface area analyzer, Fourier transform infra red (FTIR) and Raman spectroscopy. Loading of iodide and sulfur was evident from the EDAX graphs. The adsorption properties of Hg{sup 2+} as a function of pH, contact time and initial metal concentration were characterized by Cold vapor AAS. The adsorption kinetics fitted the Pseudo second order kinetics and equilibrium was reached within 90 min. The experimental data were modeled with Langmuir, Freundlich, Dubinin-Redushkevich and Temkin isotherms and various isotherm parameters were evaluated. It was found that the mercury adsorption capacity for the prepared adsorbents were in the order of CNT-S > CNT-I > CNT-OX > CNT. Studies have been conducted to demonstrate the applicability of the sorbent toward the removal of Hg(0) from broken compact fluorescent light (CFL) bulbs and Hg(II) from contaminated water streams.

  11. Recovery of mercury from mercury compounds via electrolytic methods

    Science.gov (United States)

    Grossman, Mark W.; George, William A.

    1988-01-01

    A process for electrolytically recovering mercury from mercury compounds is provided. In one embodiment, Hg is recovered from Hg.sub.2 Cl.sub.2 employing as the electrolyte solution a mixture of HCl and H.sub.2 O. In another embodiment, Hg is electrolytically recovered from HgO wherein the electrolyte solution is comprised of glacial acetic acid and H.sub.2 O. Also provided is an apparatus for producing isotopically enriched mercury compounds in a reactor and then transporting the dissolved compounds into an electrolytic cell where mercury ions are electrolytically reduced and elemental mercury recovered from the mercury compounds.

  12. The Adsorption Mechanism of Modified Activated Carbon on Phenol

    Directory of Open Access Journals (Sweden)

    Lin J. Q.

    2016-01-01

    Full Text Available Modified activated carbon was prepared by thermal treatment at high temperature under nitrogen flow. The surface properties of the activated carbon were characterized by Boehm titration, BET and point of zero charge determination. The adsorption mechanism of phenol on modified activated carbon was explained and the adsorption capacity of modified activated carbon for phenol when compared to plain activated carbon was evaluated through the analysis of adsorption isotherms, thermodynamic and kinetic properties. Results shows that after modification the surface alkaline property and pHpzc value of the activated carbon increase and the surface oxygen-containing functional groups decrease. The adsorption processes of the plain and modified carbon fit with Langmuir isotherm equation well, and the maximum adsorption capacity increase from 123.46, 111.11, 103.09mg/g to 192.31, 178.57, 163,93mg/g under 15, 25 and 35°C after modification, respectively. Thermodynamic parameters show that the adsorption of phenol on activated carbon is a spontaneously exothermic process of entropy reduction, implying that the adsorption is a physical adsorption. The adsorption of phenol on activated carbon follows the pseudo-second-order kinetics (R2>0.99. The optimum pH of adsorption is 6~8.

  13. Mercury cycling in terrestrial watersheds

    Science.gov (United States)

    Shanley, James B.; Bishop, Kevin; Banks, Michael S.

    2012-01-01

    This chapter discusses mercury cycling in the terrestrial landscape, including inputs from the atmosphere, accumulation in soils and vegetation, outputs in streamflow and volatilization, and effects of land disturbance. Mercury mobility in the terrestrial landscape is strongly controlled by organic matter. About 90% of the atmospheric mercury input is retained in vegetation and organic matter in soils, causing a buildup of legacy mercury. Some mercury is volatilized back to the atmosphere, but most export of mercury from watersheds occurs by streamflow. Stream mercury export is episodic, in association with dissolved and particulate organic carbon, as stormflow and snowmelt flush organic-rich shallow soil horizons. The terrestrial landscape is thus a major source of mercury to downstream aquatic environments, where mercury is methylated and enters the aquatic food web. With ample organic matter and sulfur, methylmercury forms in uplands as well—in wetlands, riparian zones, and other anoxic sites. Watershed features (topography, land cover type, and soil drainage class) are often more important than atmospheric mercury deposition in controlling the amount of stream mercury and methylmercury export. While reductions in atmospheric mercury deposition may rapidly benefit lakes, the terrestrial landscape will respond only over decades, because of the large stock and slow turnover of legacy mercury. We conclude with a discussion of future scenarios and the challenge of managing terrestrial mercury.

  14. 载硫活性炭脱除天然气中单质汞的研究%Remove elemental mercury by sulfur-impregnated activated carbon in natural gas

    Institute of Scientific and Technical Information of China (English)

    吕维阳; 刘盛余; 能子礼超; 汪雪婷; 吴萧

    2016-01-01

    在固定床反应装置上考察了商业载硫活性炭脱除天然气中气态 Hg0的吸附性能、影响因素、再生方法以及吸附动力学,同时结合BET,FTIR,XRD等表征手段提出载硫活性炭脱汞机理.结果表明,空速对脱汞效率限制作用有限,空速从12000h-1提高至48000h-1,脱除率变化范围在 7%以内.增加汞浓度在初始阶段可以提高其脱汞率,增加单位质量活性炭对汞的吸附量,提高温度会增加吸附体系内的活化分子,提高脱汞率,温度在80℃时效果最优,但是温度过高则会产生负面效应.不同阶段的动力学拟合结果表明化学吸附是整个吸附过程的控制步骤.热脱附实验表明载硫活性炭的脱汞温度是在 300~450℃,再生后对汞的吸附能力减弱,其原因可归为再生过程中碳硫键的损失和活性炭二次碳化时表面的烧蚀.%The adsorption performance, influence factors, regeneration method and the adsorption dynamics of the gaseous Hg0 in natural gas removed by commercial sulfur-loaded activated carbon were studied on fixed reacting device. Meanwhile, the removal mercury mechanism of S-loaded activated carbon was put forward by applying characterization methods, including BET, FTIR, XRD and etc. The result showed that the restriction effect of airspeed on removal mercury efficiency was limited. In the initial stage, removal mercury rate and adsorption capacity of element mercury can be raised by increasing mercury concentration. As temperature gets higher, the activated molecule in the system get higher and the removal mercury rate will be promoted. The best effect appeared at 80℃. But when temperature was higher than 80℃, negative effects arose. Dynamic fitting in different stages showed that chemical adsorption was the controlling step of the whole process. Besides, the thermal desorption experiment showed that the removal mercury temperature of s-loaded activated carbon ranged from 300℃ to 450℃, and the

  15. Mercury exposure in Ireland

    DEFF Research Database (Denmark)

    Cullen, Elizabeth; Evans, David S; Davidson, Fred;

    2014-01-01

    BACKGROUND: Monitoring of human exposure to mercury is important due to its adverse health effects. This study aimed to determine the extent of mercury exposure among mothers and their children in Ireland, and to identify factors associated with elevated levels. It formed part of the Demonstration...... of a study to Coordinate and Perform Human Biomonitoring on a European Scale (DEMOCOPHES) pilot biomonitoring study. METHODS: Hair mercury concentrations were determined from a convenience sample of 120 mother/child pairs. Mothers also completed a questionnaire. Rigorous quality assurance within DEMOCOPHES...... guaranteed the accuracy and international comparability of results. RESULTS: Mercury was detected in 79.2% of the samples from mothers, and 62.5% of children's samples. Arithmetic mean levels in mothers (0.262 µg/g hair) and children (0.149 µg /g hair) did not exceed the US EPA guidance value. Levels were...

  16. The tectonics of Mercury

    International Nuclear Information System (INIS)

    The probable tectonic history of Mercury and the relative sequence of events are discussed on the basis of data collected by the Mariner-10 spacecraft. Results indicate that Mercury's tectonic activity was confined to its early history; its endogenic activity was principally due to a small change in the shape of its lithosphere, caused by tidal despinning, and a small change in area caused by shrinkage due to cooling. Exogenic processes, in particular the impact activity, have produced more abundant tectonic features. Many features associated with the Caloris basin are due to loading of Mercury's thick lithosphere by extrusive lavas or subsidence due to magma withdrawal. It is emphasized that tectonic features observed on Mercury yield insight into the earliest tectonic events on planets like Mars and, perhaps, the earth, where subsequent events obscured or erased the most ancient tectonic records

  17. Mercury analysis in hair

    DEFF Research Database (Denmark)

    Esteban, Marta; Schindler, Birgit K; Jiménez-Guerrero, José A;

    2015-01-01

    Human biomonitoring (HBM) is an effective tool for assessing actual exposure to chemicals that takes into account all routes of intake. Although hair analysis is considered to be an optimal biomarker for assessing mercury exposure, the lack of harmonization as regards sampling and analytical...... assurance program (QAP) for assessing mercury levels in hair samples from more than 1800 mother-child pairs recruited in 17 European countries. To ensure the comparability of the results, standard operating procedures (SOPs) for sampling and for mercury analysis were drafted and distributed to participating...... laboratories. Training sessions were organized for field workers and four external quality-assessment exercises (ICI/EQUAS), followed by the corresponding web conferences, were organized between March 2011 and February 2012. ICI/EQUAS used native hair samples at two mercury concentration ranges (0...

  18. Nitrate Adsorption on Clay Kaolin: Batch Tests

    OpenAIRE

    Morteza Mohsenipour; Shamsuddin Shahid; Kumars Ebrahimi

    2015-01-01

    Soils possessing kaolin, gibbsite, goethite, and hematite particles have been found to have a natural capacity to attenuate pollution in aqueous phase. On the other hand, the hydroxyl group in soil increases anion exchange capacity under a low pH condition. The main objective of this paper was to evaluate effects of kaolin on nitrate reduction under acidic condition. In order to analyze the kaolin adsorption behaviour under various conditions, four different concentrations of nitrate, 45, 112...

  19. Ecosystem conceptual model- Mercury

    Science.gov (United States)

    Alpers, Charles N.; Eagles-Smith, Collin A.; Foe, Chris; Klasing, Susan; Marvin-DiPasquale, Mark C.; Slotton, Darell G.; Windham-Myers, Lisamarie

    2008-01-01

    Mercury has been identified as an important contaminant in the Delta, based on elevated concentrations of methylmercury (a toxic, organic form that readily bioaccumulates) in fish and wildlife. There are health risks associated with human exposure to methylmercury by consumption of sport fish, particularly top predators such as bass species. Original mercury sources were upstream tributaries where historical mining of mercury in the Coast Ranges and gold in the Sierra Nevada and Klamath-Trinity Mountains caused contamination of water and sediment on a regional scale. Remediation of abandoned mine sites may reduce local sources in these watersheds, but much of the mercury contamination occurs in sediments stored in the riverbeds, floodplains, and the Bay- Delta, where scouring of Gold-Rush-era sediment represents an ongoing source.Conversion of inorganic mercury to toxic methylmercury occurs in anaerobic environments including some wetlands. Wetland restoration managers must be cognizant of potential effects on mercury cycling so that the problem is not exacerbated. Recent research suggests that wettingdrying cycles can contribute to mercury methylation. For example, high marshes (inundated only during the highest tides for several days per month) tend to have higher methylmercury concentrations in water, sediment, and biota compared with low marshes, which do not dry out completely during the tidal cycle. Seasonally inundated flood plains are another environment experiencing wetting and drying where methylmercury concentrations are typically elevated. Stream restoration efforts using gravel injection or other reworking of coarse sediment in most watersheds of the Central Valley involve tailings from historical gold mining that are likely to contain elevated mercury in associated fines. Habitat restoration projects, particularly those involving wetlands, may cause increases in methylmercury exposure in the watershed. This possibility should be evaluated.The DRERIP

  20. Mercury in human hair

    International Nuclear Information System (INIS)

    The analysis of mercury (Hg) in scalp hair obtained from individuals residing in five different localities in the Philippines - Metro Manila, Naga City in Bicol, Bataan, Oriental Mindoro, and Palawan is presented. An overall mean of 1.46 ug/g of hair was obtained for all samples excluding those from Palawan and represents a baseline value.'' In terms of the mercury levels found in hair, the Honda Bay area in Palawan is, relatively, a ''contaminated area.'' (author)

  1. Mercury CEM Calibration

    Energy Technology Data Exchange (ETDEWEB)

    John F. Schabron; Joseph F. Rovani; Susan S. Sorini

    2007-03-31

    The Clean Air Mercury Rule (CAMR) which was published in the Federal Register on May 18, 2005, requires that calibration of mercury continuous emissions monitors (CEMs) be performed with NIST-traceable standards. Western Research Institute (WRI) is working closely with the Electric Power Research Institute (EPRI), the National Institute of Standards and Technology (NIST), and the Environmental Protection Agency (EPA) to facilitate the development of the experimental criteria for a NIST traceability protocol for dynamic elemental mercury vapor generators. The traceability protocol will be written by EPA. Traceability will be based on the actual analysis of the output of each calibration unit at several concentration levels ranging from about 2-40 ug/m{sup 3}, and this analysis will be directly traceable to analyses by NIST using isotope dilution inductively coupled plasma/mass spectrometry (ID ICP/MS) through a chain of analyses linking the calibration unit in the power plant to the NIST ID ICP/MS. Prior to this project, NIST did not provide a recommended mercury vapor pressure equation or list mercury vapor pressure in its vapor pressure database. The NIST Physical and Chemical Properties Division in Boulder, Colorado was subcontracted under this project to study the issue in detail and to recommend a mercury vapor pressure equation that the vendors of mercury vapor pressure calibration units can use to calculate the elemental mercury vapor concentration in an equilibrium chamber at a particular temperature. As part of this study, a preliminary evaluation of calibration units from five vendors was made. The work was performed by NIST in Gaithersburg, MD and Joe Rovani from WRI who traveled to NIST as a Visiting Scientist.

  2. Defluoridation of drinking water using adsorption processes

    International Nuclear Information System (INIS)

    Highlights: ► Comprehensive and critical literature review on various adsorbents used for defluoridation. ► pH, temperature, kinetics and co-existing anions effects on F adsorption. ► Choice of adsorbents for various circumstances. ► Adsorption thermodynamics and mechanisms. ► Future research on efficient, low cost adsorbents which are easily regenerated. -- Abstract: Excessive intake of fluoride (F), mainly through drinking water, is a serious health hazard affecting humans worldwide. There are several methods used for the defluoridation of drinking water, of which adsorption processes are generally considered attractive because of their effectiveness, convenience, ease of operation, simplicity of design, and for economic and environmental reasons. In this paper, we present a comprehensive and a critical literature review on various adsorbents used for defluoridation, their relative effectiveness, mechanisms and thermodynamics of adsorption, and suggestions are made on choice of adsorbents for various circumstances. Effects of pH, temperature, kinetics and co-existing anions on F adsorption are also reviewed. Because the adsorption is very weak in extremely low or high pHs, depending on the adsorbent, acids or alkalis are used to desorb F and regenerate the adsorbents. However, adsorption capacity generally decreases with repeated use of the regenerated adsorbent. Future research needs to explore highly efficient, low cost adsorbents that can be easily regenerated for reuse over several cycles of operations without significant loss of adsorptive capacity and which have good hydraulic conductivity to prevent filter clogging during the fixed-bed treatment process

  3. Mechanism of amitriptyline adsorption on Ca-montmorillonite (SAz-2)

    Energy Technology Data Exchange (ETDEWEB)

    Chang, Po-Hsiang [Department of Earth Sciences, National Cheng Kung University, 1 University Road, Tainan 70101, Taiwan (China); Jiang, Wei-Teh, E-mail: atwtj@mail.ncku.edu.tw [Department of Earth Sciences, National Cheng Kung University, 1 University Road, Tainan 70101, Taiwan (China); Li, Zhaohui, E-mail: li@uwp.edu [Department of Geosciences, University of Wisconsin – Parkside, 900 Wood Road, Kenosha, WI 53144 (United States); Kuo, Chung-Yih [Department of Public Health, College of Health Care and Management, Chung Shan Medical University, No. 110, Sec. 1, Chien-kuo N Road, Taichung 40242, Taiwan (China); Jean, Jiin-Shuh [Department of Earth Sciences, National Cheng Kung University, 1 University Road, Tainan 70101, Taiwan (China); Chen, Wan-Ru [Department of Environmental Engineering, National Cheng Kung University, 1 University Road, Tainan 70101, Taiwan (China); Lv, Guocheng [School of Materials Science and Technology, China University of Geosciences, Beijing 100083 (China)

    2014-07-30

    Graphical abstract: XRD patterns to show AMI intercalation into SAz-2 vs. direct mixing of the same amount of AMI with SAz-2. - Highlights: • Ca-montmorillonite is proven to be an efficient adsorbent or sink for amitriptyline. • The high adsorption capacity is accompanied with intercalation into interlayers. • The adsorption is mainly governed by a cation exchange mechanism. • Horizontal mono- and bi-layer conformations occur at low and high adsorption levels. • The process is an endothermic physisorption at high adsorption levels. - Abstract: The uptake of amitriptyline (AMI) from aqueous environment by Ca-montmorillonite (SAz-2) was studied in a batch system under different physicochemical conditions. The adsorbent was characterized by X-ray diffraction and Fourier transform infrared (FTIR) analyses. The AMI adsorption on SAz-2 obeyed the Langmuir isotherm with a capacity of 330 mg/g (1.05 mmol/g) at pH 6–7. The adsorption kinetics was fast, almost reaching equilibrium in 2 h, and followed a pseudo-second-order kinetic model. Desorption of exchangeable cations correlated with the AMI adsorption well, indicating that cation exchange was the major mechanism. X-ray diffraction patterns showing significant expansions of the d{sub 0} {sub 0} {sub 1} spacing and characteristic FTIR band shifts toward higher frequencies after AMI adsorption onto SAz-2 indicated that the adsorbed AMI molecules were intercalated into the interlayers of the mineral. Thermodynamic parameters based on partitioning coefficients suggested that the AMI adsorption was an endothermic physisorption at high adsorption levels. At low and higher AMI adsorption levels, the intercalated AMI molecules take a horizontal monolayer and bilayer conformation, respectively. The higher adsorption capacity suggested that SAz-2 could be a good candidate to remove AMI from wastewater and would be an important environmental sink for the fate and transport of AMI in soils and groundwater.

  4. Subtask 2.7 -- Mercury capture on solid surfaces and aerosols. Semi-annual report, July 1--December 31, 1996

    Energy Technology Data Exchange (ETDEWEB)

    Schultz, R.L.

    1997-08-01

    Determining the fly ash properties responsible for the capture of mercury in coal-fired power generation systems is key to understanding and controlling mercury emissions in these systems. Several capture mechanisms and interactions may be possible, such as condensation, chemical adsorption, physical adsorption, chemical bonding, and amalgamation. The chemical nature of the exposed surfaces and the amount of surface area are likely to affect the amount of mercury capture, so both of these parameters must be explored. Since much of the fly ash surface area is concentrated on submicron particles, the interaction of mercury with submicron particles needs to be evaluated. Another possible explanation of mercury capture on fly ash is the formation of amalgams with other metal species that may be present in the fly ash; if this is true, amalgamation may be a viable control technology. The project objectives are to relate mercury capture by fly ash to chemical and physical properties of the fly ash, determine mercury associations with submicron aerosols, evaluate mercury capture on metal sorbents, and relate experimental results to predictions based on state-of-the-art models. Results to date on these activities are described.

  5. Contribution of Ash Content Related to Methane Adsorption Behaviors of Bituminous Coals

    Directory of Open Access Journals (Sweden)

    Yanyan Feng

    2014-01-01

    Full Text Available Methane adsorption isotherms on coals with varying ash contents were investigated. The textural properties were characterized by N2 adsorption/desorption isotherm at 77 K, and methane adsorption characteristics were measured at pressures up to 4.0 MPa at 298 K, 313 K, and 328 K, respectively. The Dubinin-Astakhov model and the Polanyi potential theory were employed to fit the experimental data. As a result, ash content correlated strongly to methane adsorption capacity. Over the ash range studied, 9.35% to 21.24%, the average increase in methane adsorption capacity was 0.021 mmol/g for each 1.0% rise in ash content. With the increasing ash content range of 21.24%~43.47%, a reduction in the maximum adsorption capacities of coals was observed. In addition, there was a positive correlation between the saturated adsorption capacity and the specific surface area and micropore volume of samples. Further, this study presented the heat of adsorption, the isosteric heat of adsorption, and the adsorbed phase specific heat capacity for methane adsorption on various coals. Employing the proposed thermodynamic approaches, the thermodynamic maps of the adsorption processes of coalbed methane were conducive to the understanding of the coal and gas simultaneous extraction.

  6. Mercury pollution in Malaysia.

    Science.gov (United States)

    Hajeb, Parvaneh; Jinap, S; Ismail, Ahmad; Mahyudin, Nor Ainy

    2012-01-01

    Although several studies have been published on levels of mercury contamination of the environment, and of food and human tissues in Peninsular Malaysia, there is a serious dearth of research that has been performed in East Malaysia (Sabah and Sarawak). Industry is rapidly developing in East Malaysia, and, hence, there is a need for establishing baseline levels of mercury contamination in environmental media in that part of the country by performing monitoring studies. Residues of total mercury and inorganic in food samples have been determined in nearly all previous studies that have been conducted; however, few researchers have analyzed samples for the presence of methlymercury residues. Because methylmercury is the most toxic form of mercury, and because there is a growing public awareness of the risk posed by methylmercury exposure that is associated with fish and seafood consumption, further monitoring studies on methylmercury in food are also essential. From the results of previous studies, it is obvious that the economic development in Malaysia, in recent years, has affected the aquatic environment of the country. Primary areas of environmental concern are centered on the rivers of the west Peninsular Malaysian coast, and the coastal waters of the Straits of Malacca, wherein industrial activities are rapidly expanding. The sources of existing mercury input to both of these areas of Malaysia should be studied and identified. Considering the high levels of mercury that now exists in human tissues, efforts should be continued, and accelerated in the future, if possible, to monitor mercury contamination levels in the coastal states, and particularly along the west Peninsular Malaysian coast. Most studies that have been carried out on mercury residues in environmental samples are dated, having been conducted 20-30 years ago; therefore, the need to collect much more and more current data is urgent. Furthermore, establishing baseline levels of mercury exposure to

  7. Mercury pollution in Malaysia.

    Science.gov (United States)

    Hajeb, Parvaneh; Jinap, S; Ismail, Ahmad; Mahyudin, Nor Ainy

    2012-01-01

    Although several studies have been published on levels of mercury contamination of the environment, and of food and human tissues in Peninsular Malaysia, there is a serious dearth of research that has been performed in East Malaysia (Sabah and Sarawak). Industry is rapidly developing in East Malaysia, and, hence, there is a need for establishing baseline levels of mercury contamination in environmental media in that part of the country by performing monitoring studies. Residues of total mercury and inorganic in food samples have been determined in nearly all previous studies that have been conducted; however, few researchers have analyzed samples for the presence of methlymercury residues. Because methylmercury is the most toxic form of mercury, and because there is a growing public awareness of the risk posed by methylmercury exposure that is associated with fish and seafood consumption, further monitoring studies on methylmercury in food are also essential. From the results of previous studies, it is obvious that the economic development in Malaysia, in recent years, has affected the aquatic environment of the country. Primary areas of environmental concern are centered on the rivers of the west Peninsular Malaysian coast, and the coastal waters of the Straits of Malacca, wherein industrial activities are rapidly expanding. The sources of existing mercury input to both of these areas of Malaysia should be studied and identified. Considering the high levels of mercury that now exists in human tissues, efforts should be continued, and accelerated in the future, if possible, to monitor mercury contamination levels in the coastal states, and particularly along the west Peninsular Malaysian coast. Most studies that have been carried out on mercury residues in environmental samples are dated, having been conducted 20-30 years ago; therefore, the need to collect much more and more current data is urgent. Furthermore, establishing baseline levels of mercury exposure to

  8. Mercury(II) and methyl mercury determinations in water and fish samples by using solid phase extraction and cold vapour atomic absorption spectrometry combination.

    Science.gov (United States)

    Tuzen, Mustafa; Karaman, Isa; Citak, Demirhan; Soylak, Mustafa

    2009-07-01

    A method has been developed for mercury(II) and methyl mercury speciation on Staphylococcus aureus loaded Dowex Optipore V-493 micro-column in the presented work, by using cold vapour atomic absorption spectrometry. Selective and sequential elution with 0.1 molL(-1) HCl for methyl mercury and 2 molL(-1) HCl for mercury(II) were performed at the pH range of 2-6. Optimal analytical conditions including pH, amounts of biosorbent, sample volumes were investigated. The detection limits of the analytes were 2.5 ngL(-1) for Hg(II) and 1.7 ngL(-1) for methyl mercury. The capacity of biosorbent for mercury(II) and methyl mercury was 6.5 and 5.4 mgg(-1), respectively. The validation of the presented procedure is performed by the analysis of standard reference material. The speciation procedure established was successfully applied to the speciation of mercury(II) and methyl mercury in natural water and microwave digested fish samples.

  9. Heavy metal adsorption changes of EAF steel slag after phosphorus adsorption.

    Science.gov (United States)

    Song, Guanling; Cao, Lijing; Chen, Xiao; Hou, Wenhua; Wang, Qunhui

    2012-01-01

    A kind of electric arc furnace (EAF) steel slag was phosphated, and its isothermal and dynamic adsorptions of copper, cadmium, and lead ions were measured to determine if heavy metal adsorption changes after phosphorus adsorption. The surface area increased greatly after the slag was phosphated. Isothermal adsorption experiments showed that the theoretical Q(max) of the EAF steel slag on Cu(2+), Cd(2+), and Pb(2+) improved 59, 50, and 89% respectively after it was phosphated. Dynamic adsorption results showed that the greatest adsorption capacities of unit volume of Cu(2+), Cd(2+), and Pb(2+) were 2.2, 1.8, and 1.8 times that of the column packed with original EAF steel slag when the column was packed with phosphate EAF steel slag at the same heavy metal ion concentration. The breakthrough time, the exhaustion time and elution efficiency of the column also increased when the column was packed with phosphated EAF steel slag compared with that packed with original EAF steel slag. Phosphorus adsorption could further improve the heavy metal ion adsorption of the EAF steel slag.

  10. Industrial water treatment, by adsorption, using organized mesoporous materials

    Science.gov (United States)

    Koubaissy, Bachar; Toufaily, Joumana; Kafrouny, Lina; Joly, Guy; Magnoux, Patrick; Hamieh, Tayssir

    In this work, pure silica SBA-15 was synthesized by a sol-gel method and in-situ functionalized by a series of organosilane. These mesoporous materials are used to absorb polluants from wastewater. We studied the influence of functional groups on adsorption of phenol drifts. The carboxylic acid groups and substituted chlorine on phenol have been studied. There is a sharp increase of adsorption (more than double compared to phenol) which is very encouraging. Furthermore we note that the percentage of grafted ligands also plays an important role in adsorption. Finally, the adsorption capacity also depends on the nature and percentage of ligands present.

  11. Fractal-like adsorption kinetics of Pb2+ in rocks

    Institute of Scientific and Technical Information of China (English)

    XU Longjun; ZHOU Zhengguo; LIU Chenglun; XIAN Xuefu

    2008-01-01

    The adsorption kinetics of Pb2+ in rocks has been studied using ion selective electrodes and atomic absorption spectrophotometer. The results showed that the adsorption process is a fractal-like reaction. The adsorption rate was relatively high before 30 minutes, and then dropped. The saturated adsorption capacity (a) of Pb2+ and kinetic parameters (b, α , D and k) increased with increasing initial concentrations of Pb2+. These parameters (except a) decreased while Na+ was present in the solution. Furthermore, the smaller the rocks were in grain size, the bigger these kinetic parameters would be, though the parameter a was almost constant.

  12. Adsorption of phenol from water by ultrafine coal powders

    Institute of Scientific and Technical Information of China (English)

    LIU Zhuan-nian; ZHOU An-ning; YANG Fan; JIN Qi-ting

    2007-01-01

    Seven Shenfu coal powders different in particle size obtained by sieving and ball milling were used to probe their adsorption properties to phenol from water.The results show that the kinetics of phenol on coal powders follow the second-Order adsorption kinetic model well.Adsorption processes are governed by film diffusion and the kinetic parameters and the effective diffusion coefficients were calculated through plotting.Adsorption capacities to phenol increase exponentially with decreasing of diameter of coal described in terms of Freundlich isotherm,while for ultrafine coal powders with d50 of 4.28and 4.82 μm fit Langmuir isotherm well.

  13. Removal of copper by modified chitosan adsorptive membrane

    Institute of Scientific and Technical Information of China (English)

    Xiaoshuai LIU; Zihong CHENG; Wei MA

    2009-01-01

    In this study, a novel adsorptive membrane was prepared from chitosan as the functional polymer and some additive blend solutions by solution casting method.The modified chitosan membrane was characterized by FTIR and its Water Swelling Ratio (WSR). The adsorption of copper ions on the adsorptive membrane was investi-gated in batch experiments. The results obtained from the experiments indicated that the membrane had a good adsorption capacity for copper ions, the optimal ionic strength and pH were 0.1 and 5-6, respectively. Compared with the Langmuir isotherm model, the experimental data were found to be following the Freundlich model.

  14. Fluoride and lead adsorption on carbon nanotubes

    Institute of Scientific and Technical Information of China (English)

    WANG Shuguang; LI Yanhui

    2004-01-01

    The properties and applications of CNT have been studied extensively since Iijima discovered them in 1991[1,2]. They have exceptional mechanical properties and unique electrical property, highly chemical stability and large specific surface area. Thus far, they have widely potential applications in many fields. They can be used as reinforcing materials in composites[3], field emissions[4], hydrogen storage[5], nanoelectronic components[6], catalyst supports[7], adsorption material and so on. However, the study on the potential application of CNT, environmental protection field in particular, was hardly begun.Long[8] et al. reported that CNT had a significantly higher dioxin removal efficiency than that of activated carbon. The Langmuir adsorption constant is 2.7 × 1052, 1.3 × 1018 respectively. The results indicated that CNT is potential candidate for the removal of micro-organic pollutants. However, the reports on the CNT used as fluoride and heavy metal adsorbent are seldom.In this paper, A novel material, alumina supported on carbon nanotubes (Al2O3/CNT), was prepared from carbon nanotubes and Al(NO3)3. X-ray diffraction (XRD) spectra demonstrate that alumina is amorphous, and scanning electron microscope (SEM) images show that CNT and alumina are homogeneously mixed. Furthermore, the fluoride adsorption behavior on the surface of Al2O3/CNT has been investigated and compared with other adsorbents. The results indicate that Al2O3/CNT has a high adsorption capacity, with a saturation adsorption capacity of 39.4 mg/g. It is also found that the adsorption capacity of Al2O3/CNT is 3.0~4.5 times that of γ-Al2O3while almost equal to that of IRA-410 polymeric resin at 25 ℃. The adsorption isotherms of fluoride on Al2O3/CNT is fit the Freundlich equation well, optimal pH ranging from 5.0 to 9.0.Also in this paper, a novel material, modified carbon nanotubes (CNT), was prepared from carbon nanotubes and HNO3 under boiling condition. Infrared spectroscopy (IR

  15. Adsorption kinetics,isotherm,and thermodynamic studies of adsorption of pollutant from aqueous solutions onto humic acid

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    In the present study,humic acid was used as an adsorbent for the investigation of the adsorption kinetics,isotherms,and thermo-dynamic parameters of hexavalent chromium from aqueous solution at varying pH,temperatures,and concentrations.Adsorption isotherms and equilibrium adsorption capacities were determined by the fittings of the experimental data to three well-known iso-therm models:Langmuir,Freundlich,and Redlich-Peterson.The results showed that the Langmuir and Redlich-Peterson models appear to fit the adsorption better than did the Freundlich adsorption model for the adsorption of chromium onto humic acid.The equilibrium constants were used to calculate thermodynamic parameters such as the change of free energy,enthalpy,and entropy.The derived adsorption constants (logaL) and their temperature dependencies from Langmuir isotherm have been used to calculate the corresponding thermodynamic quantities such as the free energy of adsorption,heat,and entropy of adsorption.The thermo-dynamic data indicate that Cr (VI) adsorption onto humic acid is entropically driven and characterized by physical adsorption.

  16. Characteristics of Phosphorous Adsorption and Desorption by Organo-Mineral Colloidal Complexes of Purple Paddy Soils

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The kinetic characteristics of P adsorption and desorption by organo-mineral colloidal complexes (OMC)were studied using acid, calcareous and neutral purple paddy soils taken from Chongqing and Sichuan, China.The results showed that the P adsorption capacity of the organo-mineral colloidal complexes differed with the soil types, being higher for the acid and calcareous purple soils than for the neutral purple soils. Partial removal of the organic matter increased the adsorption capacity of the colloidal complexes. A very significant positive correlation was found between the amounts of P desorbed from OMC and the P saturation degrees.The P adsorption reaction was quick at the early stage and slowed later. The raise of temperature increased P adsorption capacity and P adsorption rate of the colloidal complexes. The adsorption processes could be described by the Elovich equation.

  17. Adsorption of Pb(II by Activated Pyrolytic Char from Used Tire

    Directory of Open Access Journals (Sweden)

    Lu Ping

    2016-01-01

    Full Text Available As a renewable resource, the pyrolytic char derived from used tire has promising adsorption capacities owing to its similar structure and properties with active carbon. The purification and activation of the pyrolytic char from used tire, as well as the application of this material in the adsorption of Pb(II in water is conducted. The influences on the adsorption capacity by temperature and pH value are investigated and discussed; the adsorption thermodynamics and kinetics are also studied. The results show that the pyrolytic char from used tire has remarkable adsorption capacity for Pb(II, and the adsorption is an endothermic process complying with the Langmuir isotherm. The adsorption kinetics is a pseudo second-order reaction.

  18. Adsorptive removal of Congo red, a carcinogenic textile dye, from aqueous solutions by maghemite nanoparticles

    International Nuclear Information System (INIS)

    The adsorption of Congo red (CR) onto maghemite nanoparticles (γ-Fe2O3) and its desorption was investigated. The adsorption capacity was evaluated using both the Langmuir and Freundlich adsorption isotherm models. Maghemite nanoparticles (γ-Fe2O3) were prepared easily in a surfactant-less microemulsion by co-precipitation method. The size of the produced maghemite nanoparticles was determined by X-ray diffraction (XRD) analysis and scanning electron microscopy (SEM). Synthesized maghemite nanoparticles showed the highest adsorption capacities of CR compared to many other adsorbents and would be a good method to increase adsorption efficiency for the removal of CR in a wastewater treatment process. The maximum adsorption occurred at pH 5.9. The Langmuir adsorption capacity (qmax) was found to be 208.33 mg g-1 of the adsorbent.

  19. 壳聚糖金属离子印迹树脂的吸附模型%ADSORPTION MODEL OF METAL ION ON IMPRINTING CHITOSAN RESIN

    Institute of Scientific and Technical Information of China (English)

    谭天伟; 贺小进; 杜卫霞

    2001-01-01

    Adsorption model of metal ion on imprinting chitosan resin wasstudied. The chemical and the physical properties such as pore size distribution and heat stability were discussed and the imprinting chitosan resin can be used many times without losing adsorption capacity. The adsorption isotherms and adsorption mechanism were studied and a new model was suggested to correlate relation of adsorption with pH and metal ion concentration,which could explain mechanism of adsorption.

  20. Sorbent-based gaseous mercury removal from flue gas in hybrid particulate collector

    Energy Technology Data Exchange (ETDEWEB)

    H.K. Choi; Y.J. Rhim; S.D. Kim; Lee, S.H. Lee; S.S. Kim [Korea Institute of Energy Research, Daejeon (Republic of Korea)

    2007-07-01

    In this study, the hybrid particulate collector on the gaseous mercury removal performance was estimated. Hybrid particulate collector consists of sorbent injection/adsorption reactor, electrostatic precipitator and fabric filters. The hybrid particulate collector acts not only as a particulate collector but also as an adsorption reactor. Activated carbons injected in the flue gas in front of the injection/adsorption reactor, floating inside of the particulate collector and that attached on the inner walls take important role in mercury removal respectively, and also the activated carbons being attached on the filter surface do. Since the collector itself plays as an adsorption reactor, high mercury removal efficiency can be attained at the low C/Hg ratio. Overall removal efficiency was about 60%. When considering the baseline mercury removal efficiency was over the 50% in the coal fired power plants and MSW incinerators, it could be possible to obtain removal efficiency over the 90% with this hybrid particulate collector. 6 refs., 8 figs., 1 tab.

  1. Activated Carbon Adsorption Properties of the Residual Matters in Textile Dyeing and Printing Secondary Effluent

    Institute of Scientific and Technical Information of China (English)

    TIAN Qing; LI Fang; LIU Fang; YANG Bo; CHEN Ji-hua

    2008-01-01

    The research employed the adsorption isotherm measurement, the batch kinetic adsorption and the rapid small-scale carbon column test (RSSCT) to find out the characteristics and main impacting factors of granular activated carbon (GAC) adsorption, in treating the textile dyeing-printing/polyester alkali de-weighting secondary effluent (TSE). The adsorption affinities and capacities for the organics surrogated by CODCr, color and UV254 (UV absorbency at λ= 254 nm) predicted by isotherm, small-scale-fixed bed were discussed. Adsorption rates for CODCr, color and UV254 are much different and carbon particle size dependent. The color adsorption rate and capacity should be taken as the main consideration factors in designing bio-activated carbon filter(BACF). The breakthrough of GAC adsorption column is mainly influenced by the low MW readily adsorbable organics in TSE. UVm is a good adsorption breakthrough indicator. The study provides References for BACFs' design and operation control in textile secondary effluent (TSE) tertiary treatment.

  2. Evaluation of Thermodynamic Parameters of 2, 4-Dichlorophenoxyacetic Acid (2, 4-D Adsorption

    Directory of Open Access Journals (Sweden)

    A. S. Ghatbandhe

    2013-01-01

    Full Text Available Thermodynamic parameters of 2, 4-Dichlorophenoxyacetic acid (2, 4-D adsorption were evaluated by studying the adsorption equilibrium and kinetics of 2, 4-D at different temperatures. Uptake capacity of activated carbon increases with temperature. Langmuir isotherm models were applied to experimental data of 2, 4-D adsorption. Equilibrium data fitted very well to the Langmuir equilibrium model. Adsorbent monolayer capacity , Langmuir constant and adsorption rate constant were evaluated at different temperatures for activated carbon adsorption. The activation energy of adsorption ( was determined using the Arrhenius equation. Using the thermodynamic equilibrium coefficients obtained at different temperatures, the thermodynamic constants of adsorption (, , and were evaluated. The obtained values of thermodynamic parameters show that the adsorption of 2, 4-D is an endothermic process.

  3. Adsorption of Monobutyl Phthalate from Aqueous Phase onto Two Macroporous Anion-Exchange Resins

    Directory of Open Access Journals (Sweden)

    Zhengwen Xu

    2014-01-01

    Full Text Available As new emerging pollutants, phthalic acid monoesters (PAMs pose potential ecological and human health risks. In the present study, adsorption performance of monobutyl phthalate (MBP onto two macroporous base anion-exchange resins (D-201 and D-301 was discussed. It was found that the adsorption isotherms were best fitted by the Langmuir equation while the adsorption kinetics were well described by pseudo-first-order model. Analyses of sorption isotherms and thermodynamics proved that the adsorption mechanisms for DBP onto D-201 were ion exchange. However, the obtained enthalpy values indicate that the sorption process of MBP onto D-301 is physical adsorption. The equilibrium adsorption capacities and adsorption rates of DBP on two different resins increased with the increasing temperature of the solution. D-301 exhibited a higher adsorption capacity of MBP than D-201. These results proved that D-301, as an effective sorbent, can be used to remove phthalic acid monoesters from aqueous solution.

  4. Adsorption of hexavalent chromium by graphite–chitosan binary composite

    Indian Academy of Sciences (India)

    RAJENDRA S DONGRE

    2016-06-01

    Graphite chitosan binary (GCB) composite was prepared for hexavalent chromium adsorption from studied water. GCB was characterized by TGA, FTIR, SEM and X-ray diffraction techniques.Wide porous sorptive surface of 3.89 m$^2$ g$^{−1}$ and absorptive functionalities of GCB was due to 20% (w/w) graphite support on chitosan evidenced from FTIR and SEM that impart maximum adsorption at pH 4, agitation with 200 rpm for 180 min. Adsorption studies revealed intraparticle diffusion models and best-fitted kinetics was pseudo 2nd order one. A wellfitted Langmuir isotherm model suggested monolayer adsorption with an adsorption capacity ($q_m$) of 105.6 mg g$^{−1}$ and $R^2 = 0.945$. Sorption mechanisms based on metal ionic interactions, intrusion/diffusion and chemisorptions onto composite. This graphite chitosan binary composite improve sorbent capacity for Cr(VI).

  5. Adsorptive Removal of Dye from Industrial Effluents Using Natural Iraqi Palygorskite Clay as Low-Cost Adsorbent

    OpenAIRE

    Dakhil Nasir Taha; Isra'a Sadi Samaka; Luma Ahmed Mohammed

    2013-01-01

    Palygorskite clay has been investigated as low cost and ecofriendly adsorbent for the removal Basic Red 2(BR-2) from aqueous solution. Batch adsorption studies are carried out by observing effect of amount of adsorbent dose, contact time, pH, initial concentration of ( BR-2) and particle size of adsorbent on the adsorption capacity of the adsorbent were studied. Adsorption data fits the Langmuir and Freundlich adsorption isotherms. The calculated value of the Langmuir parameter for adsorption...

  6. Use of statistical design of experiments to evaluate the sorption capacity of 7-amine-4-azaheptylsilica and 10-amine- 4-azadecylsilica for Cu(II), Pb(II), and Fe(III) adsorption.

    Science.gov (United States)

    Passos, Camila G; Ribaski, Fernanda S; Simon, Nathália M; dos Santos, Araci A; Vaghetti, Júlio C P; Benvenutti, Edilson V; Lima, Eder Cláudio

    2006-10-15

    7-Amine-4-azaheptylsilica (AAH Si) and 10-amine-4-azadecylsilica (AAD Si) were prepared and used for removal of Cu(II), Pb(II), and Fe(III) from aqueous solutions. Full 2(3) factorial designs with two pseudo-central points were carried out in order to achieve the best conditions of the batch adsorption procedure for metallic ion uptake by the adsorbents. To continue the optimizations, central composite surface design was also employed. These two independent statistical designs of experiments lead to the following conditions: m=30.0 mg of adsorbent; pH 6.0 for Cu(II) and Pb(II), pH 4.0 for Fe(III); t of contact 180 min to guarantee equilibration at higher adsorbate concentration. After optimization of the conditions, isotherms of the metallic ions adsorbed on the AAH Si and AAD Si adsorbents were obtained, which were fitted to nonlinear Langmuir and Freundlich isotherm models.

  7. Mercury's magnetic field and interior

    International Nuclear Information System (INIS)

    The magnetic-field data collected on Mercury by the Mariner-10 spacecraft present substantial evidence for an intrinsic global magnetic field. However, studies of Mercury's thermal evolution show that it is most likely that the inner core region of Mercury solidified or froze early in the planet's history. Thus, the explanation of Mercury's magnetic field in the framework of the traditional planetary dynamo is less than certain

  8. Elemental mercury exposure: peripheral neurotoxicity.

    OpenAIRE

    Levine, S P; Cavender, G D; Langolf, G D; Albers, J W

    1982-01-01

    Nerve conduction tests were performed on the right ulnar nerve of factory workers exposed to elemental mercury vapour. Time integrated urine mercury indices were used to measure the degree of exposure. Workers with prolonged distal latencies had significantly higher urine mercury concentrations when compared with those with normal latencies. Significant correlations between increasing urine mercury concentrations and prolonged motor and sensory distal latencies were established. Elemental mer...

  9. Experimental study on gas permeability by adsorption under 3D-stress

    Institute of Scientific and Technical Information of China (English)

    LONG Qing-ming; WEN Guang-cai; ZOU Yin-hui; ZHAO Xu-sheng

    2009-01-01

    Using self-developed gas-seepage experimental installation, under the same effective stress conditions, coal permeability experiments on different adsorption charac-teristics of gases, different temperatures and different gas adsorption contents were per-formed, and the influence law of adsorption on coal permeability was studied. At the same time, experimental analogy showed clearly that gas drawing plucks the permeability varia-tion law. The results show that adsorption has a major impact on coal permeability. The greater the adsorption, the more the gas adsorption capacity and the coal permeability becomes smaller. Permeability becomes smaller along with confining of pressure and temperature, and this is in accord with local practice results.

  10. Mercury (Environmental Health Student Portal)

    Science.gov (United States)

    ... Water Waterborne Diseases & Illnesses Water Cycle Water Treatment Mercury The Basics Mercury — sometimes called quicksilver — is a natural metal. It’s ... to breathe it in without knowing it. When mercury combines with other chemical elements, it creates compounds, ...

  11. Mercury content of edible mushrooms

    Energy Technology Data Exchange (ETDEWEB)

    Woidich, H.; Pfannhauser, W.

    1975-05-01

    The mercury content of edible fungi is different. Relatively high burdened are Boletus and Agaricus campestris. A minimum of mercury is found in Russula, Agaricus bisporus and Cantharellus cibarius. The possibilities of mercury uptake and the potential cumulation mechanism is discussed. 8 references, 3 tables.

  12. Sensing Mercury for Biomedical and Environmental Monitoring

    Directory of Open Access Journals (Sweden)

    Julia Xiaojun Zhao

    2009-07-01

    Full Text Available Mercury is a very toxic element that is widely spread in the atmosphere, lithosphere, and surface water. Concentrated mercury poses serious problems to human health, as bioaccumulation of mercury within the brain and kidneys ultimately leads to neurological diseases. To control mercury pollution and reduce mercury damage to human health, sensitive determination of mercury is important. This article summarizes some current sensors for the determination of both abiotic and biotic mercury. A wide array of sensors for monitoring mercury is described, including biosensors and chemical sensors, while piezoelectric and microcantilever sensors are also described. Additionally, newly developed nanomaterials offer great potential for fabricating novel mercury sensors. Some of the functional fluorescent nanosensors for the determination of mercury are covered. Afterwards, the in vivo determination of mercury and the characterization of different forms of mercury are discussed. Finally, the future direction for mercury detection is outlined, suggesting that nanomaterials may provide revolutionary tools in biomedical and environmental monitoring of mercury.

  13. Adsorption studies of methylene blue dye on tunisian activated lignin

    Science.gov (United States)

    Kriaa, A.; Hamdi, N.; Srasra, E.

    2011-02-01

    Activated carbon prepared from natural lignin, providing from a geological deposit, was used as the adsorbent for the removal of methylene blue (MB) dye from aqueous solutions. Batch adsorption studies were conducted to evaluate various experimental parameters like pH and contact time for the removal of this dye. Effective pH for MB removal was 11. Kinetic study showed that the adsorption of dye was gradual process. Quasi equilibrium reached in 4 h. Pseudo-first-order, pseudo-second-order were used to fit the experimental data. Pseudo-second-order rate equation was able to provide realistic description of adsorption kinetics. The experimental isotherms data were also modelled by the Langmuir and Freundlich equation of adsorption. Equilibrium data fitted well with the Langmuir model with maximum monolayer adsorption capacity of 147 mg/g. Activated lignin was shown to be a promising material for adsorption of MB from aqueous solutions.

  14. Adsorption and desorption kinetics of carbofuran in acid soils.

    Science.gov (United States)

    Bermúdez-Couso, Alipio; Fernández-Calviño, David; Pateiro-Moure, Miriam; Nóvoa-Muñoz, Juan Carlos; Simal-Gándara, Jesús; Arias-Estévez, Manuel

    2011-06-15

    Carbofuran adsorption and desorption were investigated in batch and stirred flow chamber (SFC) tests. The carbofuran adsorption capacity of the soils was found to be low and strongly dependent on their clay and organic carbon contents. Carbofuran sorption was due mainly (>80%) to fast adsorption processes governed by intraparticle diffusion. The adsorption kinetic constant for the pesticide ranged from 0.047 to 0.195 min(-1) and was highly correlated with constant n in the Freundlich equation (r=0.965, Pcarbofuran desorption to be highly variable and negatively correlated with eCEC and the clay content. The SFC tests showed that soil organic carbon (C) plays a key role in the irreversibility of carbofuran adsorption. Carbofuran desorption increased rapidly at C contents below 4%. The desorption kinetic constant for the compound (0.086-0.195 min(-1)) was generally higher than its adsorption kinetic constant; therefore, carbofuran is more rapidly desorbed than it is adsorbed in soil.

  15. Modelling of copper and zinc adsorption onto zeolite

    Directory of Open Access Journals (Sweden)

    H. Pavolová

    2016-10-01

    Full Text Available Adsorption of Cu(II and Zn(II ions from metallurgical solutions has been studied and the adsorption capacity of zeolite (Nižný Hrabovec, SK has been determined. Zeolites are characterized by relatively high sorption capacity, i.e. Cu(II and Zn(II can be removed even at relatively low concentrations. The experiments were realised in a batch system and evaluated using isotherms. According to the results of the experiments the adsorption equilibrium of Cu(II and Zn(II on zeolite was best described by Freundlich isotherm. The maximum sorption capacity was 1,48 and 1,49 mg/g for Cu(II and Zn(II, respectively. The experimental results of this study demonstrate that zeolite is suitable for adsorption of copper and zinc from aqueous solutions at low concentrations.

  16. Phytoremediation of mercury-contaminated soils by Jatropha curcas.

    Science.gov (United States)

    Marrugo-Negrete, José; Durango-Hernández, José; Pinedo-Hernández, José; Olivero-Verbel, Jesús; Díez, Sergi

    2015-05-01

    Jatropha curcas plants species were tested to evaluate their phytoremediation capacity in soils contaminated by different levels of mercury. The experimental treatments consisted of four levels of mercury concentrations in the soil - T0, T1, T5, and T10 (0, 1, 5, and 10 μg Hg per g soil, respectively). The total mercury content absorbed by the different plant tissues (roots, stems and leaves) was determined during four months of exposure. The growth behavior, mercury accumulation, translocation (TF) and bioconcentration (BCF) factors were determined. The different tissues in J. curcas can be classified in order of decreasing accumulation Hg as follows: roots>leaves>stems. The highest cumulative absorption of the metal occurred between the second and third month of exposure. Maximum TF was detected during the second month and ranged from 0.79 to 1.04 for the different mercury concentrations. Values of BCF ranged from 0.21 to 1.43. Soils with T1 showed significantly higher BCF (1.43) followed by T10 (1.32) and T5 (0.91), all of them at the fourth month. On the other hand TFs were low (range 0.10-0.26) at the en of the experiment. The maximum reduction of biomass (16.3%) occurred for T10 (10 μg Hg g(-1)). In sum, J. curcas species showed high BCFs and low TFs, and their use could be a promising approach to remediating mercury-contaminated soils.

  17. Phytoremediation of mercury-contaminated soils by Jatropha curcas.

    Science.gov (United States)

    Marrugo-Negrete, José; Durango-Hernández, José; Pinedo-Hernández, José; Olivero-Verbel, Jesús; Díez, Sergi

    2015-05-01

    Jatropha curcas plants species were tested to evaluate their phytoremediation capacity in soils contaminated by different levels of mercury. The experimental treatments consisted of four levels of mercury concentrations in the soil - T0, T1, T5, and T10 (0, 1, 5, and 10 μg Hg per g soil, respectively). The total mercury content absorbed by the different plant tissues (roots, stems and leaves) was determined during four months of exposure. The growth behavior, mercury accumulation, translocation (TF) and bioconcentration (BCF) factors were determined. The different tissues in J. curcas can be classified in order of decreasing accumulation Hg as follows: roots>leaves>stems. The highest cumulative absorption of the metal occurred between the second and third month of exposure. Maximum TF was detected during the second month and ranged from 0.79 to 1.04 for the different mercury concentrations. Values of BCF ranged from 0.21 to 1.43. Soils with T1 showed significantly higher BCF (1.43) followed by T10 (1.32) and T5 (0.91), all of them at the fourth month. On the other hand TFs were low (range 0.10-0.26) at the en of the experiment. The maximum reduction of biomass (16.3%) occurred for T10 (10 μg Hg g(-1)). In sum, J. curcas species showed high BCFs and low TFs, and their use could be a promising approach to remediating mercury-contaminated soils. PMID:25655698

  18. Determination of binding capacity and adsorption enthalpy between Human Glutamate Receptor (GluR1) peptide fragments and kynurenic acid by surface plasmon resonance experiments. Part 2: Interaction of GluR1270-300 with KYNA.

    Science.gov (United States)

    Csapó, E; Bogár, F; Juhász, Á; Sebők, D; Szolomájer, J; Tóth, G K; Majláth, Z; Vécsei, L; Dékány, I

    2015-09-01

    In the course of our previous work, the interactions of two peptide fragments (GluR1201-230 and GluR1231-259) of human glutamate receptor (GluR1201-300) polypeptide with kynurenic acid (KYNA) were investigated by surface plasmon resonance (SPR) spectroscopy. Besides quantitation of the interactions, the enthalpies of binding of KYNA on certain peptide fragment-modified gold surfaces were also reported. In the present work, a third peptide fragment (GluR1270-300) of the glutamate receptor was synthesized and its interaction with KYNA was investigated by an SPR technique. This 31-membered peptide was chemically bonded onto a gold-coated SPR chip via a cysteine residue. The peptide-functionalized biosensor chip was analyzed by atomic force microscopy (AFM) and theoretical calculations were performed on the structure and dimensions of the peptide on the gold surface. In order to determine the isosteric heat of adsorption of the binding of KYNA on the peptide-functionalized gold thin film, SPR experiments were carried out between +10°C and +40°C. The results on the GluR1270-300-KYNA system were compared with the previously published binding parameters of the interactions of GluR1201-230 and GluR1231-259 with KYNA. The binding abilities of KYNA with all three peptide fragments immobilized on the gold surface were estimated by a molecular docking procedure and the binding free energies of these AMPA receptor subunits with KYNA were determined.

  19. Sensing Mercury for Biomedical and Environmental Monitoring

    OpenAIRE

    Julia Xiaojun Zhao; E. Michael Collins; Hanying Xu; Selid, Paul D.; Marla Striped Face-Collins

    2009-01-01

    Mercury is a very toxic element that is widely spread in the atmosphere, lithosphere, and surface water. Concentrated mercury poses serious problems to human health, as bioaccumulation of mercury within the brain and kidneys ultimately leads to neurological diseases. To control mercury pollution and reduce mercury damage to human health, sensitive determination of mercury is important. This article summarizes some current sensors for the determination of both abiotic and biotic mercury. A wid...

  20. Microemulsion synthesis of hydroxyapatite nanomaterials and their adsorption behaviors for Cr3+ ions

    Science.gov (United States)

    Gao, Y. L.; Wang, X. S.; Cui, H. H.; Mu, M. M.; Huang, F. Z.

    2016-05-01

    Hydroxyapatite (HAP) nanoparticles with different morphologies, such as nanorods, nanospheres, and their mixtures were successfully synthesized by microemulsion method with soluble additive. Their adsorption capacity for Cr3+ ion was investigated. Most of the Cr3+ were absorbed by HAP within 60 min. The adsorption capacity of the HAP nanospheres was the best, and the maximum Cr3+ removal ratio was 96.4%, revealing that the metal ions adsorption by HAP is dependent on the morphology of its particles.

  1. Modeling of Experimental Adsorption Isotherm Data

    Directory of Open Access Journals (Sweden)

    Xunjun Chen

    2015-01-01

    Full Text Available Adsorption is considered to be one of the most effective technologies widely used in global environmental protection areas. Modeling of experimental adsorption isotherm data is an essential way for predicting the mechanisms of adsorption, which will lead to an improvement in the area of adsorption science. In this paper, we employed three isotherm models, namely: Langmuir, Freundlich, and Dubinin-Radushkevich to correlate four sets of experimental adsorption isotherm data, which were obtained by batch tests in lab. The linearized and non-linearized isotherm models were compared and discussed. In order to determine the best fit isotherm model, the correlation coefficient (r2 and standard errors (S.E. for each parameter were used to evaluate the data. The modeling results showed that non-linear Langmuir model could fit the data better than others, with relatively higher r2 values and smaller S.E. The linear Langmuir model had the highest value of r2, however, the maximum adsorption capacities estimated from linear Langmuir model were deviated from the experimental data.

  2. Adsorptive removal of Cu(II) from aqueous solutions using collagen-tannin resin

    International Nuclear Information System (INIS)

    The collagen-tannin resin (CTR), as a novel adsorbent, was prepared via a reaction of collagen with black wattle tannin and aldehyde, and its adsorption properties to Cu(II) were systematically investigated, including pH effect, adsorption equilibrium, adsorption kinetics, and column adsorption. The adsorption capacity of Cu(II) on CTR was pH-dependent, and it increased with the increase of solution pH. The adsorption isotherms were well described by Langmuir isotherm model with correlating constant (R2) higher than 0.99. The adsorption capacity determined at 303 K was high up to 0.26 mmol/g, which was close to the value (0.266 mmol/g) estimated from Langmuir equation. The adsorption capacity was increased with the increase of temperature, and thermodynamic calculations suggested that the adsorption of Cu(II) on CTR is an endothermic process. The adsorption kinetics were well fitted by the pseudo-second-order rate model. Further column studies suggested that CTR was effective for the removal of Cu(II) from solutions, and more than 99% of Cu(II) was desorbed from column using 0.1 mol/L HNO3 solution. The CTR column can be reused to adsorb Cu(II) without any loss of adsorption capacity.

  3. Adsorptive removal of Cu(II) from aqueous solutions using collagen-tannin resin

    Energy Technology Data Exchange (ETDEWEB)

    Sun Xia; Huang Xin [Department of Biomass Chemistry and Engineering, Sichuan University, Chengdu 610065 (China); Liao Xuepin, E-mail: xpliao@scu.edu.cn [Department of Biomass Chemistry and Engineering, Sichuan University, Chengdu 610065 (China); National Engineering Laboratory for Clean Technology of Leather Manufacture, Sichuan University, Chengdu 610065 (China); Shi Bi, E-mail: shibi@scu.edu.cn [National Engineering Laboratory for Clean Technology of Leather Manufacture, Sichuan University, Chengdu 610065 (China)

    2011-02-28

    The collagen-tannin resin (CTR), as a novel adsorbent, was prepared via a reaction of collagen with black wattle tannin and aldehyde, and its adsorption properties to Cu(II) were systematically investigated, including pH effect, adsorption equilibrium, adsorption kinetics, and column adsorption. The adsorption capacity of Cu(II) on CTR was pH-dependent, and it increased with the increase of solution pH. The adsorption isotherms were well described by Langmuir isotherm model with correlating constant (R{sup 2}) higher than 0.99. The adsorption capacity determined at 303 K was high up to 0.26 mmol/g, which was close to the value (0.266 mmol/g) estimated from Langmuir equation. The adsorption capacity was increased with the increase of temperature, and thermodynamic calculations suggested that the adsorption of Cu(II) on CTR is an endothermic process. The adsorption kinetics were well fitted by the pseudo-second-order rate model. Further column studies suggested that CTR was effective for the removal of Cu(II) from solutions, and more than 99% of Cu(II) was desorbed from column using 0.1 mol/L HNO{sub 3} solution. The CTR column can be reused to adsorb Cu(II) without any loss of adsorption capacity.

  4. Mercury radar speckle dynamics

    Science.gov (United States)

    Holin, Igor V.

    2010-06-01

    Current data reveal that Mercury is a dynamic system with a core which has not yet solidified completely and is at least partially decoupled from the mantle. Radar speckle displacement experiments have demonstrated that the accuracy in spin-dynamics determination for Earth-like planets can approach 10 -5. The extended analysis of space-time correlation properties of radar echoes shows that the behavior of speckles does not prevent estimation of Mercury's instantaneous spin-vector components to accuracy of a few parts in 10 7. This limit can be reached with more powerful radar facilities and leads to constraining the interior in more detail from effects of spin dynamics, e.g., from observation of the core-mantle interplay through high precision monitoring of the 88-day spin-variation of Mercury's crust.

  5. Water displacement mercury pump

    Science.gov (United States)

    Nielsen, Marshall G.

    1985-01-01

    A water displacement mercury pump has a fluid inlet conduit and diffuser, a valve, a pressure cannister, and a fluid outlet conduit. The valve has a valve head which seats in an opening in the cannister. The entire assembly is readily insertable into a process vessel which produces mercury as a product. As the mercury settles, it flows into the opening in the cannister displacing lighter material. When the valve is in a closed position, the pressure cannister is sealed except for the fluid inlet conduit and the fluid outlet conduit. Introduction of a lighter fluid into the cannister will act to displace a heavier fluid from the cannister via the fluid outlet conduit. The entire pump assembly penetrates only a top wall of the process vessel, and not the sides or the bottom wall of the process vessel. This insures a leak-proof environment and is especially suitable for processing of hazardous materials.

  6. Adsorption on mixtures of ion exchangers

    International Nuclear Information System (INIS)

    A theoretical study has been made of adsorption on mixtures of ion exchangers. The effect of variables such as the concentration of the ion being adsorbed, the concentration of the supporting electrolyte, loading, the values of the capacities and equilibrium constants for the various exchange processes, and the fraction of each adsorber in the mixture on the observed distribution coefficient has been investigated. A computer program has been written to facilitate the calculation of distribution coefficients for the adsorption of an ion on a given mixture of ion exchangers under a specified set of conditions

  7. Adsorption of Lead Ions by Linde type F(K Zeolite

    Directory of Open Access Journals (Sweden)

    Han Chenghui

    2016-01-01

    Full Text Available The Test was to examine the adsorption property of Pb(II irons by Linde type F (K zeolite. The zeolite was synthesized by fly ash. The adsorbent dosage, pH, reaction temperature and reaction time were investigated. The adsorption isotherm and adsorption kinetics equation were studied. The results showed the adsorbent dosage, pH, reaction temperature and reaction time had significant effects on the adsorption of Pb(II irons. The removal rate was improved with the increasing of zeolite dosage. The saturated adsorption capacity was decreased gradually. The adsorption of Pb(II irons tended to saturate when initial pH was 6. With the increasing of temperature, the equilibration time of adsorption was shorter. Langmuir isotherm was more applicable to explain the monolayer adsorption procedure of Pb(II on Linde type F(K zeolite. For adsorption kinetics, pseudo-second order model showed better calculation results.

  8. Efficient adsorption of phenanthrene by simply synthesized hydrophobic MCM-41 molecular sieves

    Science.gov (United States)

    Hu, Yun; He, Yinyun; Wang, Xiaowen; Wei, Chaohai

    2014-08-01

    Hydrophobic molecular sieve MCM-41 including surfactant template was synthesized by a simple method. The adsorption properties of this material toward phenanthrene were studied. The effects of adsorbent dose and pH value on the adsorption process as well as the adsorption mechanism and reuse performance were investigated. The template-containing MCM-41 showed a significant adsorption for phenanthrene, due to its hydrophobicity created by the surfactant template in MCM-41. The solution pH had little effect on the adsorption capacity. The adsorption kinetic could be fitted well with pseudo-second-order kinetic model. The adsorption equilibrium was fitted well by the linear model, and the adsorption process followed the liquid/solid phase distribution mechanism. The thermodynamic results indicated that the adsorption was a spontaneous and exothermic process.

  9. Study on the adsorption kinetics of orthophosphate anions on layer double hydroxide

    Institute of Scientific and Technical Information of China (English)

    PENG Shuchuan; L(U) Lü; WANG Jin; HAN Lu; CHEN Tianhu; JIANG Shaotong

    2009-01-01

    A kinetic study was conducted on the adsorption of orthophosphate anions on layer double hydroxide (LDH). The adsorption has proved itself to be a spontaneous endothermic process and is large in capacity and rate. The adsorption isotherm correlates well with the Freundlich model, and a rise in temperature will lead to an increase in adsorption efficiency. Additionally, the results suggested that the adsorption is an entropy-increasing process and is in good agreement with the pseudo-second order kinetics. The free energy (ΔG) of adsorption of orthophosphate onto LDH varies within the range of -1.75- -3.34 kJ/mol, the enthalpy (ΔH) varies by 7.96 kJ/mol and the entropy (ΔS) by 33.59 kJ/mol. The adsorption activation energy is 8.3 kJ/mol, showing that the adsorption of orthophosphate onto LDH is determined to be a physical adsorption.

  10. The Sun, Mercury, and Venus

    CERN Document Server

    Elkins-Tanton, Linda T

    2010-01-01

    The Messenger mission to Mercury opened a new window into the inner solar system. In 2008, this mission began a number of years of flybys, culminating in an orbital insertion around Mercury and producing unparalleled observations about this mysterious innermost planet. Mercury orbits so close to the Sun, from the point of view of Earth, that seeing it from the Earth against the Sun's glare is a great challenge. At the same time, the huge gravitational force of the Sun makes it a challenge to put a mission on Mercury without losing it into the Sun. Now, with heightened understanding of Mercury,

  11. Interfacial adsorption of insulin - Conformational changes and reversibility of adsorption

    NARCIS (Netherlands)

    Mollmann, SH; Jorgensen, L; Bukrinsky, JT; Elofsson, U; Norde, W; Frokjaer, S

    2006-01-01

    The adsorption of human insulin to Teflon particles was studied with respect to conformational changes and the reversibility of adsorption was examined by total internal reflection fluorescence (TIRF). Adsorption isotherms for the adsorption of human insulin indicated high affinity adsorption, even

  12. Interfacial adsorption of insulin. Conformational changes and reversibility of adsorption

    NARCIS (Netherlands)

    Mollmann, S.H.; Bukrinsky, J.T.; Elofsson, U.; Norde, W.; Frokjaer, S.

    2006-01-01

    The adsorption of human insulin to Teflon particles was studied with respect to conformational changes and the reversibility of adsorption was examined by total internal reflection fluorescence (TIRF). Adsorption isotherms for the adsorption of human insulin indicated high affinity adsorption, even

  13. Effect of aging process on adsorption of diethyl phthalate in soils amended with bamboo biochar.

    Science.gov (United States)

    Zhang, Xiaokai; Sarmah, Ajit K; Bolan, Nanthi S; He, Lizhi; Lin, Xiaoming; Che, Lei; Tang, Caixian; Wang, Hailong

    2016-01-01

    Biochar is a carbonaceous sorbent and can be used as a potential material to reduce the bioavailability of organic pollutants in contaminated soils. In the present study, the adsorption and desorption of diethyl phthalate (DEP) onto soils amended with bamboo biochar was investigated with a special focus on the effect of biochar application rates and aging conditions on the adsorption capacity of the soils. Biochar amendment significantly enhanced the soil adsorption of DEP that increased with increasing application rates of biochar. However, the adsorption capacity decreased by two aging processes (alternating wet and dry, and constantly moist). In the soil with low organic carbon (OC) content, the addition of 0.5% biochar (without aging) increased the adsorption by nearly 98 times compared to the control, and exhibited the highest adsorption capacity among all the treatments. In the soil with high OC content, the adsorption capacity in the treatment of 0.5% biochar without aging was 3.5 and 3 times greater than those of the treatments of biochar aged by alternating wet and dry, and constantly moist, respectively. Moreover, constantly moist resulted in a greater adsorption capacity than alternating wet and dry treatments regardless of biochar addition. This study revealed that biochar application enhanced soil sorption of DEP, however, the enhancement of the adsorption capacity was dependent on the soil organic carbon levels, and aging processes of biochar.

  14. The adsorption capacity of Pb2+ by waste collagen fiber spun-lace fabric tannins immobilized%单宁固化废鞣革胶原水刺布的 Pb2+吸附性能

    Institute of Scientific and Technical Information of China (English)

    赵继松; 殷保璞

    2014-01-01

    The waste leather was made into waste collagen fiber spun-lace fabric by textile manufacturing process. This kind of spun-lace fabric was then immobilized by tannin through the cross-link of glutaraldehyde. The structure and strength of the fabric were studied.Then the influences of initial Pb2+concentration, the temperature and pH value of the solution on the absorption of Pb2+have been studied.It shows that with the increase of these three parameters, adsorption of Pb2+increases,up to 25.95 mg/g.Finally, the fabric that has absorbed Pb2+was treated by 0.1 mol/L HCl solution to study its properties of de-sorption and performance of recycling.%将制革工业中的废弃皮革经过非织造工艺制成废鞣革胶原水刺布,通过戊二醛交联将单宁固化到废鞣革胶原水刺布上。首先研究单宁固化废鞣革胶原水刺布的形态结构及强伸性变化,然后分别研究Pb2+的初始浓度、溶液温度、溶液pH值对Pb2+吸附量的影响。结果表明:随着Pb2+的初始浓度、溶液温度、溶液pH值的增大,Pb2+的吸附量逐渐增大,最大为25.95 mg/g。最后利用0.1 mol/L稀HCl溶液对吸附材料进行解吸附试验,并讨论单宁固化废鞣革胶原水刺布吸附材料的解吸附性能及再生性。

  15. Plane Mercury librations

    Science.gov (United States)

    Barkin, Yu. V.; Ferrandiz, J. M.

    2009-04-01

    Introduction. In 1988 I. Kholin [1] has developed a precision method of determination of parameters of rotation of planets on complex radar-tracking observations on two radio telescopes making base and definitely carried on surface of the Earth. His American colleagues for the period approximately in 4 with small year have executed a series of radar-tracking measurements on a method and I. Kholin's program [2] and have obtained for the specified period 21 values of angular velocity of rotation of this planet [3]. With the help of numerical integration of the equations of rotary motion on the found values they managed to determine with high accuracy the basic dynamic parameter in the theory of Mercury librations (B - A)•Cm = (2.03± 0.12) × 10-4 and the corresponding to it the value of amplitude of the basic librations35"8 ± 2"1. These results have served as convincing arguments for the benefit of the Peale's assumption, that a core of Mercury is liquid, or in partially molten [4]. Authors also managed to obtain for the first time parameters of resonant librations in a longitude which opening from radar observations was predicted earlier [5]. Its amplitude makes about 300", the period is equal approximately to 12 years. In the paper [6] parameters of the perturbed rotational motion have been determined with the help of the analytical theory and with formal using of results of mentioned work [3] on determination of 21 values of angular velocity of Mercury. In result the estimations of amplitudes of forced librations of first five harmonics with the periods: 87.97 d, 43.99 d, 29.33 d, 21.99 d and 17.59 d have been obtained. The appropriate amplitudes make values:34"05 ± 1"27, 3"59 ± 0"13, 0"354 ± 0"013, 0"072 ± 0"003 and 0"016 ± 0"001. The amplitude and the period of free librations of Mercury in a longitude are determined: 290"9 ± 67"0 and 12.37 ± 0.23 yr, consequently. The phase of this variation has made28401 ± 1402. In the paper we construct the similar

  16. EVALUATING CAPACITIES OF GAC PRELOADED WITH NATURAL WATER

    Science.gov (United States)

    Adsorption studies are conducted to determine how preloading a natural groundwater onto GAC affects the adsorption of cis-1,2-dichloroexthene in small-scale and pilot-scale columns. Capacities are determined from batch-isotherm tests, microcolumns, and pilot columns, which are p...

  17. Impact of salinity and dispersed oil on adsorption of dissolved aromatic hydrocarbons by activated carbon and organoclay.

    Science.gov (United States)

    Younker, Jessica M; Walsh, Margaret E

    2015-12-15

    Adsorption capacity of phenol and naphthalene by powdered activated carbon (PAC), a commercial organoclay (OC) and a lab synthesized organoclay (BTMA) was studied using batch adsorption experiments under variable feed water quality conditions including single- and multi- solute conditions, fresh water, saline water and oily-and-saline water. Increasing salinity levels was found to reduce adsorption capacity of OC, likely due to destabilization, aggregation and subsequent removal of organoclay from the water column, but did not negatively impact adsorption capacity of PAC or BTMA. Increased dispersed oil concentrations were found to reduce the surface area of all adsorbents. This decreased the adsorption capacity of PAC for both phenol and naphthalene, and reduced BTMA adsorption of phenol, but did not negatively affect naphthalene removals by either organoclay. The presence of naphthalene as a co-solute significantly reduced phenol adsorption by PAC, but had no impact on organoclay adsorption. These results indicated that adsorption by PAC occurred via a surface adsorption mechanism, while organoclay adsorption occurred by hydrophobic or pi electron interactions. In general, PAC was more sensitive to changes in water quality than either of the organoclays evaluated in this study. However, PAC exhibited a higher adsorption capacity for phenol and naphthalene compared to both organoclays even in adverse water quality conditions. PMID:26259095

  18. 利用DMO-M离子交换树脂除去稀溶液中的汞%Removal of Mercury from Dilute Aqueous Solution Using Mercaptoacetimide of Aminophenol Resin Duolite A-7

    Institute of Scientific and Technical Information of China (English)

    C.S.Zhu(朱长生); Z.K.Duan(段正康); Z.S.Liu; G.L.Rempel

    2004-01-01

    A mercaptan - containing resin, DMO- M, with high redox capacity- 6.00 mequiv / g, prepared by reacting mercaptoacetyl chloride with the aminophenol resin Duolite A-7 in free-base form has been used to remove mercury in dilute aqueous solution. The resin has high mercury removal capacity; 1200mg/g. Sodium chloride affects the equilibrium sorption of mercury on the resin. At lower pH values, below 1.76, mercury sorption of the resin was greatly reduced. The sorbed mercury is partially removed by 2 mol/L HCl solution containing 5 % thiourea.

  19. STUDY ON THE PROPERTIES OF DIFFERENT ACTIVATED CARBON FIBERS AND THEIR ADSORPTION CHARACTERISTICS FOR FORMALDEHYDE

    Institute of Scientific and Technical Information of China (English)

    H.Q. Rong; Z.Y. Ryu; J.T. Zheng

    2001-01-01

    Porous structure and surface chemistry of activated carbon fibers obtained by differ-ent precursors and activation methods were investigated. Adsorption isotherms werecharacterized by nitrogen adsorption at 77K over a relative pressure range from 10 6to 1. The regularization method according to Density Functional Theory (DFT) wasemployed to calculate the pore size distribution in the samples. Their specific surfaceareas were calculated by BET method, micropore volume and microporous specificsurface area calculated by t-plot method and MPD by Horvath-Kawazoe equation. Mi-cropore volume of rayon-based ACF was higher than that of other samples. The staticand dynamic adsorption capacity for formaldehyde on different ACFs was determined.The results show that steam activated Rayon-based A CFs had higher adsorption capac-ity than that of steam and KOH activated PAN-A CFs. Breakthrough curves illustratedthat Rayon-ACFs had longer breakthrough time, thus they possessed higher adsorp-tion capacity for formaldehyde than that of PAN-ACFs. The entire sample had smalladsorption capacity and short breakthrough time for water. Rayon-A CFs had exccl-lent adsorption selectivity for formaldehyde than PAN-ACFs. And the samples withhigh surface areas had relatively high adsorption capacity for formaldehyde. Elementaicontent of different A CFs were performed. Rayon-based A CFs contained more oxygenthan PAN-ACFs, which may be attributed to their excellent adsorption capacity forformaldehyde.

  20. Effect of DOM Size on Organic Micropollutant Adsorption by GAC.

    Science.gov (United States)

    Kennedy, Anthony M; Summers, R Scott

    2015-06-01

    Granular activated carbon (GAC) adsorption of the micropollutants 2-methylisoborneol (MIB) and warfarin (WFN) at ng/L levels was investigated in five waters with isolated natural dissolved organic matter (DOM) held at a constant dissolved organic carbon concentration. Each water was evaluated for competitive adsorption effects based on the pretreatment of ultrafiltration, coagulation, and additional background micropollutants. Using the breakthrough with unfractionated DOM as a baseline, on average, the water with lower molecular weight (MW) DOM decreased MIB and WFN adsorption capacity by 59%, whereas the water with higher MW DOM increased MIB and WFN adsorption capacity by 64%. All waters showed similar decreasing MIB and WFN adsorption capacity with increasing empty bed contact time (EBCT), with more dramatic effects seen for the more strongly adsorbing WFN. On average, MIB and WFN adsorption kinetics were two times slower in the water with higher MW DOM compared to the water with lower MW DOM, as described by the intraparticle pore diffusion tortuosity. Increased adsorption competition from 27 micropollutants other than MIB and WFN at environmentally relevant concentrations had little to no effect on MIB and WFN breakthrough behavior. Any competitive effect from background micropollutants became indiscernible at longer EBCTs. PMID:25955134

  1. N-doped mesoporous alumina for adsorption of carbon dioxide

    Institute of Scientific and Technical Information of China (English)

    Jayshri A.Thote; Ravikrishna V.Chatti; Kartik S.Iyer; Vivek Kumar; Arti N.Valechha; Nitin K.Labhsetwar; Rajesh B.Biniwale; M.K.N.Yenkie; Sadhana S.Rayalu

    2012-01-01

    N-doped mesoporous alumina has been synthesized using chitosan as the biopolymer template.The adsorbent has been thoroughly investigated for the adsorption of CO2 from a simulated flue gas stream (15% CO2 balanced with N2) and compared with commercially available mesoporous alumina procured from SASOL,Germany.CO2 adsorption was studied under different conditions of pretreatment and adsorption temperature,inlet CO2 concentration and in the presence of oxygen and moisture.The adsorption capacity was determined to be 29.4 mg CO2/g of adsorbent at 55℃.This value was observed to be 4 times higher in comparison to that of commercial mesoporous alumina at a temperature of 55℃.Basicity of alumina surface coupled with the presence of nitrogen in template in synthesized sample is responsible for this enhanced CO2 adsorption.Adsorption capacity for CO2 was retained in the presence of oxygen; however moisture had a deteriorating effect on the adsorption capacity reducing it to nearly half the value.

  2. Influence of organobentonite structure on toluene adsorption from water solution

    Directory of Open Access Journals (Sweden)

    Nuria Vidal

    2012-12-01

    Full Text Available Due to increase water pollution by organic compound derived from hydrocarbons such as toluene, several alternative technologies for remediation of polluted water have been originated. In this work natural bentonites were modified with cetyltrimethylammonium (CTMA+ for obtaining organophilic bentonites. The obtained CTMA-bentonites would be suitable for use as adsorbents of toluene present in water. The influence of structural characteristics of CTMA-bentonites on their adsorption capacity was studied. It was shown that adsorption of toluene depended on homogeneous interlayer space associated with arrangements of CTMA+ paraffin-monolayer and bilayer models, accompanied by a high degree ordering of the carbon chain of organic cation in both arrangements. However, packing density would not have an evident influence on the retention capacity of these materials. The solids obtained were characterized by chemical analysis, X-ray diffractions and infrared spectroscopy. Toluene adsorption was measured by UV-visible spectrophotometer. Adsorption capacity was studied by determining adsorption isotherms and adsorption coefficient calculation. The adsorption isotherms were straight-line indicating a partition phenomenon of toluene between the aqueous and organic phase present in organophilic bentonites.

  3. Mercury's core evolution

    Science.gov (United States)

    Deproost, Marie-Hélène; Rivoldini, Attilio; Van Hoolst, Tim

    2016-10-01

    Remote sensing data of Mercury's surface by MESSENGER indicate that Mercury formed under reducing conditions. As a consequence, silicon is likely the main light element in the core together with a possible small fraction of sulfur. Compared to sulfur, which does almost not partition into solid iron at Mercury's core conditions and strongly decreases the melting temperature, silicon partitions almost equally well between solid and liquid iron and is not very effective at reducing the melting temperature of iron. Silicon as the major light element constituent instead of sulfur therefore implies a significantly higher core liquidus temperature and a decrease in the vigor of compositional convection generated by the release of light elements upon inner core formation.Due to the immiscibility in liquid Fe-Si-S at low pressure (below 15 GPa), the core might also not be homogeneous and consist of an inner S-poor Fe-Si core below a thinner Si-poor Fe-S layer. Here, we study the consequences of a silicon-rich core and the effect of the blanketing Fe-S layer on the thermal evolution of Mercury's core and on the generation of a magnetic field.

  4. Behavior of phenol adsorption on thermal modified activated carbon☆

    Institute of Scientific and Technical Information of China (English)

    Dengfeng Zhang; Peili Huo; Wei Liu

    2016-01-01

    Adsorption process is acknowledged as an effective option for phenolic wastewater treatment. In this work, the activated carbon (AC) samples after thermal modification were prepared by using muffle furnace. The phenol ad-sorption kinetics and equilibrium measurements were carried out under static conditions at temperature ranging from 25 to 55 °C. The test results show that the thermal modification can enhance phenol adsorption on AC samples. The porous structure and surface chemistry analyses indicate that the decay in pore morphology and decrease of total oxygen-containing functional groups are found for the thermal modified AC samples. Thus, it can be further inferred that the decrease of total oxygen-containing functional groups on the modified AC sam-ples is the main reason for the enhanced phenol adsorption capacity. For both the raw sample and the optimum modified AC sample at 900 °C, the pseudo-second order kinetics and Langmuir models are found to fit the exper-imental data very well. The maximum phenol adsorption capacity of the optimum modified AC sample can reach 144.93 mg·g−1 which is higher than that of the raw sample, i.e. 119.53 mg·g−1. Adsorption thermodynamics analysis confirms that the phenol adsorption on the optimum modified AC sample is an exothermic process and mainly via physical adsorption.

  5. Synthesis of magnetic wheat straw for arsenic adsorption

    International Nuclear Information System (INIS)

    Highlights: → This work provides a way for fabricating low-cost arsenic adsorbents using agro- or plant-residues. → The introduction of wheat straw template highly enhances the arsenic adsorption of Fe3O4. → This magnetic adsorbent can be separated and collected by magnetic control easily and rapidly. → This adsorbent can be regenerated. → - Abstract: Magnetic wheat straw (MWS) with different Fe3O4 content was synthesized by using in-situ co-precipitation method. It was characterized by powder X-ray diffraction (XRD) and vibrating sample magnetometer (VSM). This material can be used for arsenic adsorption from water, and can be easily separated by applied magnetic field. The introduction of wheat straw template highly enhanced the arsenic adsorption of Fe3O4. Among three adsorption isotherm models examined, the data fitted Langmuir model better. Fe3O4 content and initial pH value influenced its adsorption behavior. Higher Fe3O4 content corresponded to a higher adsorption capacity. In the pH range of 3-11, As(V) adsorption was decreased with increasing of pH; As(III) adsorption had the highest capacity at pH 7-9. Moreover, by using 0.1 mol L-1 NaOH aqueous solution, it could be regenerated. This work provided an efficient way for making use of agricultural waste.

  6. Mechanism of amitriptyline adsorption on Ca-montmorillonite (SAz-2).

    Science.gov (United States)

    Chang, Po-Hsiang; Jiang, Wei-Teh; Li, Zhaohui; Kuo, Chung-Yih; Jean, Jiin-Shuh; Chen, Wan-Ru; Lv, Guocheng

    2014-07-30

    The uptake of amitriptyline (AMI) from aqueous environment by Ca-montmorillonite (SAz-2) was studied in a batch system under different physicochemical conditions. The adsorbent was characterized by X-ray diffraction and Fourier transform infrared (FTIR) analyses. The AMI adsorption on SAz-2 obeyed the Langmuir isotherm with a capacity of 330mg/g (1.05mmol/g) at pH 6-7. The adsorption kinetics was fast, almost reaching equilibrium in 2h, and followed a pseudo-second-order kinetic model. Desorption of exchangeable cations correlated with the AMI adsorption well, indicating that cation exchange was the major mechanism. X-ray diffraction patterns showing significant expansions of the d001 spacing and characteristic FTIR band shifts toward higher frequencies after AMI adsorption onto SAz-2 indicated that the adsorbed AMI molecules were intercalated into the interlayers of the mineral. Thermodynamic parameters based on partitioning coefficients suggested that the AMI adsorption was an endothermic physisorption at high adsorption levels. At low and higher AMI adsorption levels, the intercalated AMI molecules take a horizontal monolayer and bilayer conformation, respectively. The higher adsorption capacity suggested that SAz-2 could be a good candidate to remove AMI from wastewater and would be an important environmental sink for the fate and transport of AMI in soils and groundwater. PMID:24373983

  7. Mercury Information Clearinghouse

    Energy Technology Data Exchange (ETDEWEB)

    Chad A. Wocken; Michael J. Holmes; Dennis L. Laudal; Debra F. Pflughoeft-Hassett; Greg F. Weber; Nicholas V. C. Ralston; Stanley J. Miller; Grant E. Dunham; Edwin S. Olson; Laura J. Raymond; John H. Pavlish; Everett A. Sondreal; Steven A. Benson

    2006-03-31

    The Canadian Electricity Association (CEA) identified a need and contracted the Energy & Environmental Research Center (EERC) to create and maintain an information clearinghouse on global research and development activities related to mercury emissions from coal-fired electric utilities. With the support of CEA, the Center for Air Toxic Metals{reg_sign} (CATM{reg_sign}) Affiliates, and the U.S. Department of Energy (DOE), the EERC developed comprehensive quarterly information updates that provide a detailed assessment of developments in the various areas of mercury monitoring, control, policy, and research. A total of eight topical reports were completed and are summarized and updated in this final CEA quarterly report. The original quarterly reports can be viewed at the CEA Web site (www.ceamercuryprogram.ca). In addition to a comprehensive update of previous mercury-related topics, a review of results from the CEA Mercury Program is provided. Members of Canada's coal-fired electricity generation sector (ATCO Power, EPCOR, Manitoba Hydro, New Brunswick Power, Nova Scotia Power Inc., Ontario Power Generation, SaskPower, and TransAlta) and CEA, have compiled an extensive database of information from stack-, coal-, and ash-sampling activities. Data from this effort are also available at the CEA Web site and have provided critical information for establishing and reviewing a mercury standard for Canada that is protective of environment and public health and is cost-effective. Specific goals outlined for the CEA mercury program included the following: (1) Improve emission inventories and develop management options through an intensive 2-year coal-, ash-, and stack-sampling program; (2) Promote effective stack testing through the development of guidance material and the support of on-site training on the Ontario Hydro method for employees, government representatives, and contractors on an as-needed basis; (3) Strengthen laboratory analytical capabilities through

  8. CO2 adsorption on chemically modified activated carbon.

    Science.gov (United States)

    Caglayan, Burcu Selen; Aksoylu, A Erhan

    2013-05-15

    CO2 adsorption capacity of a commercial activated carbon was improved by using HNO3 oxidation, air oxidation, alkali impregnation and heat treatment under helium gas atmosphere. The surface functional groups produced were investigated by diffuse reflectance infrared Fourier transform spectrometer (DRIFTS). CO2 adsorption capacities of the samples were determined by gravimetric analyses for 25-200°C temperature range. DRIFTS studies revealed the formation of carboxylic acid groups on the HNO3 oxidized adsorbents. Increased aromatization and uniform distribution of the Na particles were observed on the samples prepared by Na2CO3 impregnation onto HNO3 oxidized AC support. The adsorption capacities of the nonimpregnated samples were increased by high temperature helium treatments or by increasing the adsorption temperature; both leading to decomposition of surface oxygen groups, forming sites that can easily adsorb CO2. The adsorption capacity loss due to cyclic adsorption/desorption procedures was overcome with further surface stabilization of Na2CO3 modified samples with high temperature He treatments. With Na2CO3 impregnation the mass uptakes of the adsorbents at 20 bars and 25 °C were improved by 8 and 7 folds and at 1 bar were increased 15 and 16 folds, on the average, compared to their air oxidized and nitric acid oxidized supports, respectively. PMID:23500788

  9. Novel nano bearings constructed by physical adsorption

    Science.gov (United States)

    Zhang, Yongbin

    2015-09-01

    The paper proposes a novel nano bearing formed by the physical adsorption of the confined fluid to the solid wall. The bearing is formed between two parallel smooth solid plane walls sliding against one another, where conventional hydrodynamic lubrication theory predicted no lubricating effect. In this bearing, the stationary solid wall is divided into two subzones which respectively have different interaction strengths with the lubricating fluid. It leads to different physical adsorption and slip properties of the lubricating fluid at the stationary solid wall respectively in these two subzones. It was found that a significant load-carrying capacity of the bearing can be generated for low lubricating film thicknesses, because of the strong physical adsorption and non-continuum effects of the lubricating film.

  10. Hydrophobic nano-carrier for lysozyme adsorption

    Indian Academy of Sciences (India)

    CANAN ALTUNBAS; FULDEN ZEYNEP URAL; MURAT UYGUN; NESIBE AVCIBASI; UGUR AVCIBASI; DENIZ AKTAS UYGUN; SINAN AKGÖL

    2016-04-01

    In this work, poly(HEMA–APH) nanoparticles were synthesized by surfactant-free emulsion polymerization technique.Magnetic behaviour was introduced by simple addition of Fe$_3$O$_4$ into the polymerization medium.Characterization of the nanoparticle was carried out by FTIR, ESR, SEM, AFM and EDX analyses. These synthesized magnetic nanoparticles were used for adsorption of lysozyme. For this purpose, adsorption conditions wereoptimized and maximum lysozyme binding capacity was found to be 278.8 mg g$^{−1}$ polymer in pH 7.0 phosphate buffer at 25$^{\\circ}$C. Desorption and reusability properties of the nanoparticles were investigated and lysozyme adsorption efficiency did not change significantly at the end of the 10 successive reuses.

  11. A mercury transport and fate model (LM2-mercury) for mass budget assessment of mercury cycling in Lake Michigan

    Science.gov (United States)

    LM2-Mercury, a mercury mass balance model, was developed to simulate and evaluate the transport, fate, and biogeochemical transformations of mercury in Lake Michigan. The model simulates total suspended solids (TSS), disolved organic carbon (DOC), and total, elemental, divalent, ...

  12. 汞暴露对草鱼氧化损伤及抗氧化能力的影响%Effect of mercury on oxidative damage and antioxidant capacity of Ctenopharyngodon idellus

    Institute of Scientific and Technical Information of China (English)

    刘占才; 牛景彦; 郭彦玲; 孔祥会

    2016-01-01

    This study was aimed to investigate the effect of Hg 2+on oxidative damage and antioxidant capacity of grass carp ( Ctenopharyngodon idellus) .The experimental fish were divided into control and treatment groups .The control group fish was raised in cultivated water , while the treatment group fish was exposed to 0.5 mg· L-1 Hg2+for 24 hours first, and then transferred in cultivated water .Afterwards, they were sampled at 0 (24 h Hg2+exposure), 5, 12, 21 d to test the superoxide dismutase (SOD), catalase (CAT), glutathion and peroxidase (GPx) activities as well as glutathione ( GSH) and malondialdehyde ( MDA) contents in their gill , hepatopancreas , spleen and kid-ney.It was shown that compared with the control group , the SOD, GPx activities (0, 5 d), CAT activity (0, 5, 12 d) and GSH (5 d), MDA (5, 12, 21 d) contents in gill in treatment group increased significantly (P0.05).While, the GSH content (0 d) was lowered significantly(P<0.01),and the GSH (12 d) and MDA(0 d) contents were elevated remarkably (P<0.05).The SOD (0, 5,12 d), GPx(0 d) activities and GSH (12 d), MDA (0 d) contents in kidney in treatment group were increased significantly (P<0.05).Nevertheless,CAT (0,5,12 d) activity and GSH(0,5 d) content were decreased remarkably ( P<0.05 ) .This test indicated that for grass carp , the SOD and CAT activities of organ tissues were recovered to the normal level .In hepatopancreas , GSH content exceeded the control group level ( P<0.01 ) , and MDA content was significantly lower than that of control group ( P<0.05 ) , but the GPx activity and MDA content in gill seemed unable to recover to the level of control group in the experimental period .%将草鱼分为对照组和处理组,对照组试验期内置于正常养殖用水中饲养,处理组先暴露在Hg2+浓度为0.5 mg· L-1水体中,24 h后置于正常养殖用水中进行恢复饲养。各组分别于恢复饲养0(即Hg2+暴露24 h)、5、12、21 d取样,测定鳃、肝胰脏、

  13. Mercury Phase II Study - Mercury Behavior in Salt Processing Flowsheet

    Energy Technology Data Exchange (ETDEWEB)

    Jain, V. [Savannah River Remediation, LLC., Aiken, SC (United States); Shah, H. [Savannah River Remediation, LLC., Aiken, SC (United States). Sludge and Salt Planning; Bannochie, C. J. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Wilmarth, W. R. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2016-07-25

    Mercury (Hg) in the Savannah River Site Liquid Waste System (LWS) originated from decades of canyon processing where it was used as a catalyst for dissolving the aluminum cladding of reactor fuel. Approximately 60 metric tons of mercury is currently present throughout the LWS. Mercury has long been a consideration in the LWS, from both hazard and processing perspectives. In February 2015, a Mercury Program Team was established at the request of the Department of Energy to develop a comprehensive action plan for long-term management and removal of mercury. Evaluation was focused in two Phases. Phase I activities assessed the Liquid Waste inventory and chemical processing behavior using a system-by-system review methodology, and determined the speciation of the different mercury forms (Hg+, Hg++, elemental Hg, organomercury, and soluble versus insoluble mercury) within the LWS. Phase II activities are building on the Phase I activities, and results of the LWS flowsheet evaluations will be summarized in three reports: Mercury Behavior in the Salt Processing Flowsheet (i.e. this report); Mercury Behavior in the Defense Waste Processing Facility (DWPF) Flowsheet; and Mercury behavior in the Tank Farm Flowsheet (Evaporator Operations). The evaluation of the mercury behavior in the salt processing flowsheet indicates, inter alia, the following: (1) In the assembled Salt Batches 7, 8 and 9 in Tank 21, the total mercury is mostly soluble with methylmercury (MHg) contributing over 50% of the total mercury. Based on the analyses of samples from 2H Evaporator feed and drop tanks (Tanks 38/43), the source of MHg in Salt Batches 7, 8 and 9 can be attributed to the 2H evaporator concentrate used in assembling the salt batches. The 2H Evaporator is used to evaporate DWPF recycle water. (2) Comparison of data between Tank 21/49, Salt Solution Feed Tank (SSFT), Decontaminated Salt Solution Hold Tank (DSSHT), and Tank 50 samples suggests that the total mercury as well as speciated

  14. Adsorption of Metsulfuron and Bensulfuron on a Cationic Surfactant-Modified Paddy Soil

    Institute of Scientific and Technical Information of China (English)

    LIAO Min; XIE Xiao-Mei

    2007-01-01

    Adsorption isotherms of metsulfuron and bensulfuron on a hexadecyltrimethylammonium (HDTMA) bromide-modified paddy soil under different ionic strengths, with divalent cation Cu2+, or having different pH were studied to describe their adsorptive behavior, and to try to explain the adsorption process of a sulfonylurea compound with a carbamoylsulfamoyl group in the modified soil environment. All the adsorption isotherms fitted the Freundlich equation well, and the HDTMA treatment of paddy soil dramatically enhanced adsorption capacity of metsulfuron or bensulfuron. Also, an increase of ionic strength and the addition of divalent heavy metal cation Cu2+ on the HDTMA-modified paddy soil increased the adsorption of metsulfuron or bensulfuron. Additionally, for metsulfuron and bensulfuron in the aqueous phase, adsorption capacity of the HDTMA-modified paddy soil gradually increased with decreasing pH.

  15. ADSORPTION OF PHENOL IN NON—AQUEOUS SYSTEM BASED ON HYDROGEN—BONDING

    Institute of Scientific and Technical Information of China (English)

    XUMancai; SHIZuoqing; 等

    2000-01-01

    Two hydrogen-bonding adsorbents-macroporous crosslinked poly(P-nitrostyrene)and poly(p-vinylbenzyl amide)-were synthesized,and the adsorption property of phenol from cyclohexane solution onto the adsorbents was studied,The differential adsorption heasts for varied adsorption capacities calculated from the adsorption isotherms according to the Claperyron-Clausius equation lay in the range of hydrogen bond energy (8-50kJ/mol),The adsorption capaccity of o-nitrophenol in cyclohexane was moch less than that of phenol under the same condition.The adsorption capacity of phenol from cyclohexane onto polyacrylonitrile was much less than that onto poly(p-nitrostyrene)or poly(p-vinylbenzyl amide),All these results revealed that adsorption of phenol from cyclohexane by poly(p-nitrostyrene) or poly(p-vinylbenzyl amide)is based on hydrogen-bonding.

  16. Cellulose aerogel regenerated from ionic liquid solution for immobilized metal affinity adsorption.

    Science.gov (United States)

    Oshima, Tatsuya; Sakamoto, Toshihiko; Ohe, Kaoru; Baba, Yoshinari

    2014-03-15

    Surface morphology of cellulosic adsorbents is expected to influence the adsorption behavior of biomacromolecules. In the present study, cellulose aerogel regenerated from ionic liquid solution was prepared for use as a polymer support for protein adsorption. Iminodiacetic acid groups were introduced to the aerogel for immobilized metal affinity adsorption of proteins. A Cu(II)-immobilized iminodiacetic acid cellulose aerogel (Cu(II)-IDA-CA), which has a large specific surface area, showed a higher adsorption capacity than Cu(II)-immobilized iminodiacetic acid bacterial cellulose (Cu(II)-IDA-BC) and Cu(II)-immobilized iminodiacetic acid plant cellulose (Cu(II)-IDA-PC). In contrast, the Cu(II)-immobilized cellulosic adsorbents showed similar adsorption capacities for smaller amino acid and peptides. The results show that cellulose aerogels are useful as polymer supports with high protein adsorption capacities.

  17. Surface Modification Effects on CNTs Adsorption of Methylene Blue and Phenol

    Directory of Open Access Journals (Sweden)

    A. H. Norzilah

    2011-01-01

    Full Text Available This study compares the adsorption capacity of modified CNTs using acid and heat treatment. The CNTs were synthesized from acetone and ethanol as carbon sources, using floating catalyst chemical vapor deposition (FC-CVD method. energy-dispersive X-ray spectroscopy (EDX and Boehm method revealed the existence of oxygen functional group on the surface of CNTs. Heat modification increases the adsorption capacity of as-synthesized CNTs for methylene blue (MB and phenol by approximately 76% and 50%, respectively. However, acid modification decreases the adsorption capacity. The equilibrium adsorption data fitted the Redlich-Peterson isotherm. For the adsorption kinetic study, the experimental data obeyed the pseudo-second-order model. Both modifications methods reduced the surface area and pore volume. The studies show that the adsorption of MB and phenol onto modified CNTs is much more influenced by their surface functional group than their surface area and pore volume.

  18. Confinement Correction to Mercury Intrusion Capillary Pressure of Shale Nanopores.

    Science.gov (United States)

    Wang, Sen; Javadpour, Farzam; Feng, Qihong

    2016-01-01

    We optimized potential parameters in a molecular dynamics model to reproduce the experimental contact angle of a macroscopic mercury droplet on graphite. With the tuned potential, we studied the effects of pore size, geometry, and temperature on the wetting of mercury droplets confined in organic-rich shale nanopores. The contact angle of mercury in a circular pore increases exponentially as pore size decreases. In conjunction with the curvature-dependent surface tension of liquid droplets predicted from a theoretical model, we proposed a technique to correct the common interpretation procedure of mercury intrusion capillary pressure (MICP) measurement for nanoporous material such as shale. Considering the variation of contact angle and surface tension with pore size improves the agreement between MICP and adsorption-derived pore size distribution, especially for pores having a radius smaller than 5 nm. The relative error produced in ignoring these effects could be as high as 44%--samples that contain smaller pores deviate more. We also explored the impacts of pore size and temperature on the surface tension and contact angle of water/vapor and oil/gas systems, by which the capillary pressure of water/oil/gas in shale can be obtained from MICP. This information is fundamental to understanding multiphase flow behavior in shale systems. PMID:26832445

  19. The adsorption behavior of functional particles modified by polyvinylimidazole for Cu(II) ion

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Ruixin; Men, Jiying; Gao, Baojiao [School of Chemical Engineering and Environment, North University of China, Taiyuan (China)

    2012-03-15

    In this paper, a novel composite material the silica grafted by poly(N-vinyl imidazole) (PVI), i.e., PVI/SiO{sub 2}, was prepared using 3-methacryloxypropyl trimethoxysilane (MPS) as intermedia through the ''grafting from'' method. The adsorption behavior of metal ions by PVI/SiO{sub 2} was researched by both static and dynamic methods. Experimental results showed that PVI/SiO{sub 2} possessed very strong adsorption ability for metal ions. For different metal ions, PVI/SiO{sub 2} exhibited different adsorption abilities with the following order of adsorption capacity: Cu{sup 2+}> Cd{sup 2+}> Zn{sup 2+}. The adsorption material PVI/SiO{sub 2} was especially good at adsorbing Cu(II) ion and the saturated adsorption capacity could reach up to 49.2 mg/g. The empirical Freundlich isotherm was found to describe well the equilibrium adsorption data. Higher temperatures facilitated the adsorption process and thus increased the adsorption capacity. The pH and grafting amount of PVI had great influence on the adsorption amount. In addition, PVI/SiO{sub 2} particles had excellent eluting and regenerating property using diluted hydrochloric acid solution as eluent. The adsorption ability trended to steady during 10 cycles. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  20. Batch studies of adsorption of copper and lead on activated carbon from Eucalyptus camaldulensis Dehn. Bark

    Institute of Scientific and Technical Information of China (English)

    Phussadee Patnukao; Apipreeya Kongsuwan; Prasert Pavasant

    2008-01-01

    Powdered activated carbon (PAC) prepared from Eucalyptus camaldulensis Dehn. bark was tested for its adsorption capacity for Cu(Ⅱ) and Pb(Ⅱ). The experiment was conducted to investigate the effects of pH, contact time, initial metal concentration, and temperature. The best adsorption of both Cu(Ⅱ) and Pb(Ⅱ) occurred at pH 5, where the adsorption reached equilibrium within 45 min for the whole range of initial heavy metal concentrations (0.1-10 mmol/L). The adsorption kinetics was found to follow the pseudo-second order model where equilibrium adsorption capacities and adsorption rate constants increased with initial heavy metal concentrations. The adsorption isotherm followed Langmuir better than Freundlich models within the temperature range (25-60℃). The maximum adsorption capacities (qm) occurred at 60℃, where qm for Cu(Ⅱ) and Pb(Ⅱ) were 0.85 and 0.89 mmol/g, respectively. The enthalpies of Cu(Ⅱ) and Pb(Ⅱ) adsorption were 43.26 and 58.77 kJ/mol, respectively. The positive enthalpy of adsorption indicated an endothermic nature of the adsorption.

  1. Structure sensitivity in adsorption

    DEFF Research Database (Denmark)

    Hammer, Bjørk; Nielsen, Ole Holm; Nørskov, Jens Kehlet

    1997-01-01

    The structure sensitivity of CO adsorption on different flat, stepped, kinked and reconstructed Pt surfaces is studied using large-scale density-functional calculations. We find an extremely strong structure sensitivity in the adsorption energy with variations up to 1 eV (or 100%) from one...

  2. A Simple Adsorption Experiment

    Science.gov (United States)

    Guirado, Gonzalo; Ayllon, Jose A.

    2011-01-01

    The study of adsorption phenomenon is one of the most relevant and traditional physical chemistry experiments performed by chemistry undergraduate students in laboratory courses. In this article, we describe an easy, inexpensive, and straightforward way to experimentally determine adsorption isotherms using pieces of filter paper as the adsorbent…

  3. Mercury extrusion from linear-chain mercury compounds

    International Nuclear Information System (INIS)

    Evidence is present from differential thermal analysis to show that mercury is extruded from the linear-chain mercury compound Hg/sub 2.86/AsF6 and Hg/sub 1.91/SbF6 when cooled below 200 K. The anisotropic superconductivity observed recently in Hg/sub 2.86/AsF6 is shown to result from extruded mercury

  4. Mercury's exosphere: observations during MESSENGER's First Mercury flyby.

    Science.gov (United States)

    McClintock, William E; Bradley, E Todd; Vervack, Ronald J; Killen, Rosemary M; Sprague, Ann L; Izenberg, Noam R; Solomon, Sean C

    2008-07-01

    During MESSENGER's first Mercury flyby, the Mercury Atmospheric and Surface Composition Spectrometer measured Mercury's exospheric emissions, including those from the antisunward sodium tail, calcium and sodium close to the planet, and hydrogen at high altitudes on the dayside. Spatial variations indicate that multiple source and loss processes generate and maintain the exosphere. Energetic processes connected to the solar wind and magnetospheric interaction with the planet likely played an important role in determining the distributions of exospheric species during the flyby. PMID:18599778

  5. Mercury Poisoning Linked to Skin Products

    Science.gov (United States)

    ... Products For Consumers Home For Consumers Consumer Updates Mercury Poisoning Linked to Skin Products Share Tweet Linkedin ... situations, criminal prosecution. back to top Dangers of Mercury Exposure to mercury can have serious health consequences. ...

  6. MERCURY DEPOSITION AND LAKE QUALITY TRENDS

    Science.gov (United States)

    Watershed factors influence the differing trends in mercury residue levels. Fish mercury concentrations show positive correlations with water color, methylmercury concentrations, and plankton mercury, and negative correlations with pH and alkalinity.

  7. Adsorbent for p-phenylenediamine adsorption and removal based on graphene oxide functionalized with magnetic cyclodextrin

    International Nuclear Information System (INIS)

    Highlights: • Magnetic β-cyclodextrin-graphene oxide (MCG) show high adsorption capacity. • The maximum adsorption capacity was 1102.58 mg/g at 45 °C and pH 8. • MCG can be easily and fast extracted from water by magnetic attraction. • Removal rate of MCG could reach 98% after three times of adsorption. • Adsorption capacity of MCG remained at 81% after five cycles. - Abstract: Recently, graphene oxide (GO) based magnetic nanocomposites have been widely used in an adsorption-based process for the removal of organic pollutants from the water system. In this study, magnetic β-cyclodextrin-graphene oxide nanocomposites (MCG) were synthesized according to covalent binding of magnetic β-cyclodextrin nanoparticles onto the GO surface and the as-made nanocomposites were successfully applied as adsorbents for the adsorption and removal of p-phenylenediamines (PPD). The composition and morphology of prepared materials were characterized by Fourier infrared spectrometry (FT-IR), transmission electron microscopy (TEM), vibrating sample magnetometer (VSM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). Effects of pH, temperature, time and reusability on the adsorption of PPD were investigated, as well as the kinetics and isotherms parameters of the adsorbents were determined. The results indicated that the maximum adsorption capacity of MCG was 1102.58 mg/g at 45 °C and pH 8. The adsorption capacity remained at 81% after five cycles. Removal rate could reach 98% after three times of adsorption. The adsorption process with PPD was found that fitted pseudo-second-order kinetics equations and the Langmuir adsorption model. The results showed the MCG had a good adsorption ability to remove organic pollutants in wastewater

  8. Adsorbent for p-phenylenediamine adsorption and removal based on graphene oxide functionalized with magnetic cyclodextrin

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Dongxue; Liu, Liangliang; Jiang, Xinyu; Yu, Jingang [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China); Chen, Xiaohong [Collaborative Innovation Center of Resource-conserving & Environment-friendly Society and Ecological Civilization, Changsha, 410083 (China); Chen, Xiaoqing, E-mail: xqchen@csu.edu.cn [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China); Collaborative Innovation Center of Resource-conserving & Environment-friendly Society and Ecological Civilization, Changsha, 410083 (China)

    2015-02-28

    Highlights: • Magnetic β-cyclodextrin-graphene oxide (MCG) show high adsorption capacity. • The maximum adsorption capacity was 1102.58 mg/g at 45 °C and pH 8. • MCG can be easily and fast extracted from water by magnetic attraction. • Removal rate of MCG could reach 98% after three times of adsorption. • Adsorption capacity of MCG remained at 81% after five cycles. - Abstract: Recently, graphene oxide (GO) based magnetic nanocomposites have been widely used in an adsorption-based process for the removal of organic pollutants from the water system. In this study, magnetic β-cyclodextrin-graphene oxide nanocomposites (MCG) were synthesized according to covalent binding of magnetic β-cyclodextrin nanoparticles onto the GO surface and the as-made nanocomposites were successfully applied as adsorbents for the adsorption and removal of p-phenylenediamines (PPD). The composition and morphology of prepared materials were characterized by Fourier infrared spectrometry (FT-IR), transmission electron microscopy (TEM), vibrating sample magnetometer (VSM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). Effects of pH, temperature, time and reusability on the adsorption of PPD were investigated, as well as the kinetics and isotherms parameters of the adsorbents were determined. The results indicated that the maximum adsorption capacity of MCG was 1102.58 mg/g at 45 °C and pH 8. The adsorption capacity remained at 81% after five cycles. Removal rate could reach 98% after three times of adsorption. The adsorption process with PPD was found that fitted pseudo-second-order kinetics equations and the Langmuir adsorption model. The results showed the MCG had a good adsorption ability to remove organic pollutants in wastewater.

  9. Studies on adsorption of carbon dioxide on alkaline paper mill waste using cyclic process

    International Nuclear Information System (INIS)

    Highlights: • 9–12 h adsorption of CO2 in the 1st cycle increases cyclic CO2 adsorption of APMW. • Repeated prolonged adsorptions in cycles are feasible to capture CO2 using APMW. • Prolonged adsorption increases pores in 10–100 nm of APMW after desorption of CO2. - Abstract: The adsorption/desorption cycles of the alkaline paper mill waste (APMW) can be used to remove CO2 from coal-fired power plants. In this work, the prolonged adsorption duration treatment was used to modify CO2 capture behavior of the raw and the prewashed APMW in the multiple adsorption/desorption cycles. The effects of increased duration of adsorption and CO2 partial pressure in the first cycle on the fractional adsorption of CO2 and adsorption rate were investigated, when the raw and the prewashed APMW are employed as the sorbents. The cyclic CO2 capture behavior of APMW after the repeated prolonged adsorption in different cycles was also studied. For the raw and the prewashed APMW as the sorbents, 9–12 h adsorption of CO2 just in the 1st cycle enhances the cyclic fractional adsorption of CO2 and adsorption rate of CO2 in the 1st cycle and the subsequent cycles. The repeated prolonged adsorptions in the various cycles are more effective to increase the cyclic CO2 capture capacity of APMW than only in the 1st cycle. The longer adsorption duration results in larger area and volume of pores in 10–100 nm in diameter for CaO derived from APMW after the next cycles, which are helpful to cyclic CO2 capture of APMW. The raw and the prewashed APMW can retain high CO2 adsorption reactivity by the prolonged adsorption duration treatment in the multiple adsorption/desorption cycles

  10. Fluorocarbon adsorption in hierarchical porous frameworks

    Science.gov (United States)

    Motkuri, Radha Kishan; Annapureddy, Harsha V. R.; Vijaykumar, M.; Schaef, H. Todd; Martin, Paul F.; McGrail, B. Peter; Dang, Liem X.; Krishna, Rajamani; Thallapally, Praveen K.

    2014-07-01

    Metal-organic frameworks comprise an important class of solid-state materials and have potential for many emerging applications such as energy storage, separation, catalysis and bio-medical. Here we report the adsorption behaviour of a series of fluorocarbon derivatives on a set of microporous and hierarchical mesoporous frameworks. The microporous frameworks show a saturation uptake capacity for dichlorodifluoromethane of >4 mmol g-1 at a very low relative saturation pressure (P/Po) of 0.02. In contrast, the mesoporous framework shows an exceptionally high uptake capacity reaching >14 mmol g-1 at P/Po of 0.4. Adsorption affinity in terms of mass loading and isosteric heats of adsorption is found to generally correlate with the polarizability and boiling point of the refrigerant, with dichlorodifluoromethane >chlorodifluoromethane >chlorotrifluoromethane >tetrafluoromethane >methane. These results suggest the possibility of exploiting these sorbents for separation of azeotropic mixtures of fluorocarbons and use in eco-friendly fluorocarbon-based adsorption cooling.

  11. Selective adsorption mechanisms of antilipidemic and non-steroidal anti-inflammatory drug residues on functionalized silica-based porous materials in a mixed solute.

    Science.gov (United States)

    Suriyanon, Nakorn; Permrungruang, Jutima; Kaosaiphun, Jidanan; Wongrueng, Aunnop; Ngamcharussrivichai, Chawalit; Punyapalakul, Patiparn

    2015-10-01

    The selective adsorption mechanisms of naproxen (NAP), acetaminophen (ACT), and clofibric acid (CFA) on silica-based porous materials were examined by single and mixed-batch adsorption. Effects of the types and densities of surface functional groups on adsorption capacities were determined, including the role of hydrophobic and hydrophilic dissolved organic matters (DOMs). Hexagonal mesoporous silica (HMS), superparamagnetic HMS (HMS-SP) and SBA-15 were functionalized and applied as adsorbents. Compared with powdered activated carbon (PAC), amine-functionalized HMS had a better adsorption capacity for CFA, but PAC possessed a higher adsorption capacity for the other pharmaceuticals than HMS and its two derivatives. In contrast to PAC, the adsorption capacity of the mesoporous silicas varied with the solution pH, being highest at pH 5. Electrostatic interactions and hydrogen bonding were found to be the main mechanisms. Increase in grafted amine group density on silica surfaces can enhance the CFA adsorption capacity. Further, hydrophilic DOM can decrease CFA adsorption capacities on amino-grafted adsorbents by adsorption site competition, while hydrophobic DOM can interfere with CFA adsorption by the interaction between hydrophobic DOM and CFA. Finally, in a competitive adsorption study, the adsorption capacity of hydrophilic adsorbents for acidic pharmaceuticals varied with their pKa values. PMID:26025186

  12. Efficient adsorption of phenanthrene by simply synthesized hydrophobic MCM-41 molecular sieves

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Simply synthesized template-containing MCM-41 is used for phenanthrene adsorption. • Template-containing MCM-41 has much higher adsorption capacity than pure MCM-41. • The adsorption process follows the liquid/solid phase distribution mechanism. - Abstract: Hydrophobic molecular sieve MCM-41 including surfactant template was synthesized by a simple method. The adsorption properties of this material toward phenanthrene were studied. The effects of adsorbent dose and pH value on the adsorption process as well as the adsorption mechanism and reuse performance were investigated. The template-containing MCM-41 showed a significant adsorption for phenanthrene, due to its hydrophobicity created by the surfactant template in MCM-41. The solution pH had little effect on the adsorption capacity. The adsorption kinetic could be fitted well with pseudo-second-order kinetic model. The adsorption equilibrium was fitted well by the linear model, and the adsorption process followed the liquid/solid phase distribution mechanism. The thermodynamic results indicated that the adsorption was a spontaneous and exothermic process

  13. Efficient adsorption of phenanthrene by simply synthesized hydrophobic MCM-41 molecular sieves

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Yun, E-mail: huyun@scut.edu.cn; He, Yinyun; Wang, Xiaowen; Wei, Chaohai

    2014-08-30

    Graphical abstract: - Highlights: • Simply synthesized template-containing MCM-41 is used for phenanthrene adsorption. • Template-containing MCM-41 has much higher adsorption capacity than pure MCM-41. • The adsorption process follows the liquid/solid phase distribution mechanism. - Abstract: Hydrophobic molecular sieve MCM-41 including surfactant template was synthesized by a simple method. The adsorption properties of this material toward phenanthrene were studied. The effects of adsorbent dose and pH value on the adsorption process as well as the adsorption mechanism and reuse performance were investigated. The template-containing MCM-41 showed a significant adsorption for phenanthrene, due to its hydrophobicity created by the surfactant template in MCM-41. The solution pH had little effect on the adsorption capacity. The adsorption kinetic could be fitted well with pseudo-second-order kinetic model. The adsorption equilibrium was fitted well by the linear model, and the adsorption process followed the liquid/solid phase distribution mechanism. The thermodynamic results indicated that the adsorption was a spontaneous and exothermic process.

  14. Catalyst Additives to Enhance Mercury Oxidation and Capture

    Energy Technology Data Exchange (ETDEWEB)

    Thomas K. Gale

    2006-06-30

    Catalysis is the key fundamental ingredient to convert elemental mercury in coal-fired power stations into its oxidized forms that are more easily captured by sorbents, ESPs, baghouses, and wet scrubbers, whether the catalyst be unburned carbon (UBC) in the ash or vanadium pentoxide in SCR catalysts. This project has investigated several different types of catalysts that enhance mercury oxidation in several different ways. The stated objective of this project in the Statement of Objectives included testing duct-injection catalysts, catalyst-sorbent hybrids, and coated low-pressure-drop screens. Several different types of catalysts were considered for duct injection, including different forms of iron and carbon. Duct-injection catalysts would have to be inexpensive catalysts, as they would not be recycled. Iron and calcium had been shown to catalyze mercury oxidation in published bench-scale tests. However, as determined from results of an on-going EPRI/EPA project at Southern Research, while iron and calcium did catalyze mercury oxidation, the activity of these catalysts was orders of magnitude below that of carbon and had little impact in the short residence times available for duct-injected catalysts or catalyst-sorbent hybrids. In fact, the only catalyst found to be effective enough for duct injection was carbon, which is also used to capture mercury and remove it from the flue gas. It was discovered that carbon itself is an effective catalyst-sorbent hybrid. Bench-scale carbon-catalyst tests were conducted, to obtain kinetic rates of mercury adsorption (a key step in the catalytic oxidation of mercury by carbon) for different forms of carbon. All carbon types investigated behaved in a similar manner with respect to mercury sorption, including the effect of temperature and chlorine concentration. Activated carbon was more effective at adsorbing mercury than carbon black and unburned carbon (UBC), because their internal surface area of activated carbon was

  15. Adsorption behavior of heavy metals on biomaterials.

    Science.gov (United States)

    Minamisawa, Mayumi; Minamisawa, Hiroaki; Yoshida, Shoichiro; Takai, Nobuharu

    2004-09-01

    We have investigated adsorption of Cd(II) and Pb(II) at pH 2-6.7 onto the biomaterials chitosan, coffee, green tea, tea, yuzu, aloe, and Japanese coarse tea, and onto the inorganic adsorbents, activated carbon and zeolite. High adsorptive capabilities were observed for all of the biomaterials at pH 4 and 6.7. In the adsorption of Cd(II), blend coffee, tea, green tea, and coarse tea have comparable loading capacities to activated carbon and zeolite. Although activated carbon, zeolite, and chitosan are utilized in a variety of fields such as wastewater treatment, chemical and metallurgical engineering, and analytical chemistry, these adsorbents are costly. On the other hand, processing of the test biomaterials was inexpensive, and all the biomaterials except for chitosan were able to adsorb large amounts of Pb(II) and Cd(II) ions after a convenient pretreatment of washing with water followed by drying. The high adsorption capability of the biomaterials prepared from plant materials is promising in the development of a novel, low-cost adsorbent. From these results, it is concluded that heavy metal removal using biomaterials would be an effective method for the economic treatment of wastewater. The proposed adsorption method was applied to the determination of amounts of Cd(II) and Pb(II) in water samples. PMID:15373400

  16. Adsorption of Cadmium By Silica Chitosan

    Directory of Open Access Journals (Sweden)

    Moftah Ali

    2013-03-01

    Full Text Available The adsorption process depends on initial concentration of Cd2+ and ratio of  chitosan in adsorbent. The present study deals with the competitive adsorption of Cd2+ ion onto silica graft with chitosan. Batch adsorption experiments were performed at five different initial Cd2+ concentrations (5, 10, 15, 20 and 25 ppm, on five different proportion from silica to chitosan (100%, 95%, 85%, 75% and 65% as adsorbent at pH 5. In the recovery process, the high recovery at 0.5 mg and observed the recovery decrease with increasing the initial concentration of Cd2+, and the low recovery at 0.25 mg from Cd2+. In this study, the adsorption capacity of Cd2+ in regard to the ratio of silica and chitosan hybrid adsorbents are examined in detail. The aim of this study to explore effects of initial concentrations of Cd2+, and the ratio of silica to chitosan on the adsorption and recovery of Cd2+.

  17. Research of Porization and Adsorptions in High-Porous Adsorptive Layers of Vermiculite

    Directory of Open Access Journals (Sweden)

    K. Syrmanova

    2016-06-01

    Full Text Available Adsorption capacity of the adsorbent is dependent on the concentration of the substance in the liquid or vapor phase, its partial pressure, temperature, and the initial state of the adsorbent. At the swelling a cellular porous structure is formed, total porosity that connects with the entered number and the content of the gaseous component masses. The rheological characteristics of porous masses have the decisive effect on the porous structure. Common state for all versions of swelling is a plastic-viscous porous mass condition during their porization. The interlayer structure and inter-packet intervals may be considered as vermiculite plate micropores with dimensions of 0.3 – 1.2 nm. Vermiculite cation exchange capacity is in the range of 100-150 mEq / 100 g, i.e. from clay minerals it is one of the most interchangeable. The research results of the internal structure of adsorption layers by the adsorption isotherms means indicative of the internal surface of the porous layer is characterized by an extremely complex and developed form and can be described by means of fractal geometry. A model of the geometric structure of mica materials formed in the process of blistering during heat treatment is developed. The presented model has sufficiently general form and can be used both in the organization of systematic experimental studies of porization and adsorption in the adsorption layers of highly porous, and for the porization vermiculite optimization.

  18. Optimization of salt adsorption rate in membrane capacitive deionization.

    Science.gov (United States)

    Zhao, R; Satpradit, O; Rijnaarts, H H M; Biesheuvel, P M; van der Wal, A

    2013-04-01

    Membrane capacitive deionization (MCDI) is a water desalination technique based on applying a cell voltage between two oppositely placed porous electrodes sandwiching a spacer channel that transports the water to be desalinated. In MCDI, ion-exchange membranes are positioned in front of each porous electrode to prevent co-ions from leaving the electrode region during ion adsorption, thereby enhancing the salt adsorption capacity. MCDI can be operated at constant cell voltage (CV), or at a constant electrical current (CC). In this paper, we present both experimental and theoretical results for desalination capacity and rate in MCDI (both in the CV- and the CC-mode) as function of adsorption/desorption time, salt feed concentration, electrical current, and cell voltage. We demonstrate how by varying each parameter individually, it is possible to systematically optimize the parameter settings of a given system to achieve the highest average salt adsorption rate and water recovery. PMID:23395310

  19. A review on chitosan-based adsorptive membranes.

    Science.gov (United States)

    Salehi, Ehsan; Daraei, Parisa; Arabi Shamsabadi, Ahmad

    2016-11-01

    Membrane adsorbents have emerged as powerful and attractive tools for the removal of hazardous materials such as dyes and heavy metal ions, mainly in trace amounts, from water resources. Among membrane adsorbents, th