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Journal articles on the topic 'Mercury adsorption on Ni'

Author: Grafiati

Published: 4 June 2021

Last updated: 5 February 2022

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1

Jones, Robert G., and A. W. L. Tong. "Mercury adsorption on Ni{100}." Surface Science 188, no. 1-2 (1987): 87–106. http://dx.doi.org/10.1016/s0039-6028(87)80144-9.

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2

Singh, Nagindar K., and Robert G. Jones. "Mercury adsorption on Ni(111)." Surface Science 232, no. 3 (1990): 229–42. http://dx.doi.org/10.1016/0039-6028(90)90116-p.

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3

Singh, Nagindar K., and Robert G. Jones. "Mercury adsorption on Ni(111)." Surface Science 232, no. 3 (1990): 243–58. http://dx.doi.org/10.1016/0039-6028(90)90117-q.

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4

Jones, Robert G., and A. W. L. Tong. "Mercury adsorption on Ni{100}." Surface Science Letters 188, no. 1-2 (1987): A354. http://dx.doi.org/10.1016/0167-2584(87)90010-7.

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5

Singh, NagindarK, P. A. D. M. A. Dale, D. Bullett, and RobertG Jones. "Mercury adsorption on Ni(111)." Surface Science Letters 294, no. 3 (1993): A668. http://dx.doi.org/10.1016/0167-2584(93)91102-t.

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6

Singh, Nagindar K., P. A. D. M. A. Dale, D. Bullett, and Robert G. Jones. "Mercury adsorption on Ni(111)." Surface Science 294, no. 3 (1993): 333–48. http://dx.doi.org/10.1016/0039-6028(93)90119-5.

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7

Saryati, Saryati, and Sumardjo Sumardjo. "SQUARE WAVE CATHODIC STRIPPING VOLTAMMETRY ADSORPTIVE FOR NICKEL AND COBALT ANALYSIS." Indonesian Journal of Chemistry 6, no. 2 (2010): 161–64. http://dx.doi.org/10.22146/ijc.21753.

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The adsorptive stripping voltammetric determination of Ni and Co based on adsorption of the Ni/Co and dimethylglioxime (DMG) complex on a hanging mercury drop electrode is studied. The reduction current of the adsorbed DMG complex is measured by square wave cathodic stripping voltammetry method. The effect of various parameters such as ligand concentration, pH of supporting electrolytic, adsorption potential and adsorption time on the current peak of Ni and Co voltammogram were studied. Optimum condition of this method are supporting electrolyte pH 9, DMG concentration 5×10 -4 M, adsorption po

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8

Purwanto, Agung, and Narsito Narsito. "IMPREGNATION OF 2-MERCAPTOBENZOTHIAZOLE ON DIATOMACEOUS EARTH AND ITS APPLICATION AS MERCURY(II) ADSORBEN IN AQUEOUS MEDIUM." Indonesian Journal of Chemistry 1, no. 3 (2010): 138–44. http://dx.doi.org/10.22146/ijc.21940.

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An adsorbent was prepared by impregnating 2-mercaptobenzo-thiazole onto polystirene treated diatomaceous earth support. This adsorbent was then applied to adsorb mercury(II) in aqueous medium. The mercury(II) adsorption characteristics of the adsorbent was studied by the use of the original diatomaceous earth as reference. Interaction of mercury(II) and both of diatomaceous earth as well as MBT-diatomaceous were performed in a aqueous batch system to include the following parameters: (a) medium acidity and (b) mercury(II) adsorption characteristic on MBT-diatomaceous with and without the prese

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9

Ding, Jian Dong, Yong Fa Diao, and Heng Gen Shen. "Characters of Nickel-Loaded Activated Carbon Fibers and Adsorption Experiments of Gaseous Mercury." Advanced Materials Research 156-157 (October 2010): 1211–14. http://dx.doi.org/10.4028/www.scientific.net/amr.156-157.1211.

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Nickel was loaded on the activated carbon fiber(ACF) surface, by adsorption and sintering. In order to change the chemical functional groups on the carbon fiber surface, and increase catalytic oxidation capacity and removal efficiency of activated carbon fiber to element mercury. The samples of ACF were characterized before and after loading, using XPS and XRD. The results show that the nickel content in the ACF surface was 3.36at.%. The presence of nickel form was NiO and Ni. The adsorption ability of elemental mercury before and after modification was also studied. The breakthrough time was

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10

Veselá, H., and E. Šucman. "Determination of acrylamide in food using adsorption stripping voltammetry." Czech Journal of Food Sciences 31, No. 4 (2013): 401–6. http://dx.doi.org/10.17221/256/2012-cjfs.

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A new electroanalytical method for the determination of acrylamide in food has been developed. It was found that a complex of acrylamide and Ni<sup>2+</sup> is suitable for the electrochemical determination of acrylamide. Ammonia buffer of pH&nbsp;= 9.5 was found to provide convenient conditions for the determination. optimal concentration of Ni<sup>2+</sup> was 500&nbsp;&micro;mol/l. The sample preparation procedure was optimised. The best results were found for an ethanol/water mixture (1:2) and pH = 1.4. The samples were extracted in an ultrasound bath, a

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11

Soverna, S., R. Dressler, Ch E. Düllmann, et al. "Thermochromatographic studies of mercury and radon on transition metal surfaces." Radiochimica Acta 93, no. 1 (2005): 1–8. http://dx.doi.org/10.1524/ract.93.1.1.58298.

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AbstractIn preparation for the experimental investigation of chemical properties of element 112 model studies were conducted based on the assumed similarity of element 112 to either the noble gas Rn or the transition metal Hg, its supposed lighter homologue in group 12. The adsorption behavior of elemental Hg on the transition metals Ag, Au, Ni, Pd, and Pt were investigated experimentally by off-line gas thermochromatography. The deduced adsorption data of Hg were compared with new values calculated using the Eichler–Miedema model. The observed sequence of increasing Hg-metal-interactions for

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12

Tejada-Tovar, Candelaria, Angel Villabona-Ortíz, Ángel Dario González-Delgado, and María Jiménez-Villadiego. "Kinetics of Mercury and Nickel Adsorption Using Chemically Pretreated Cocoa (Theobroma cacao) Husks." Transactions of the ASABE 62, no. 2 (2019): 461–66. http://dx.doi.org/10.13031/trans.13133.

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Abstract. Agroindustrial wastes have been widely used to prepare adsorbents for heavy metal removal because of their low cost, accessibility, and high efficiency. This work focuses on preparing a novel material from cocoa ( L.) husk residual biomass chemically modified with sodium hydroxide for used as a biosorbent for nickel and mercury uptake. The cocoa husk residual biomass was characterized by FT-IR analysis to test the diversification of functional groups. The effect of particle size on removal yield was evaluated through batch adsorption experiments. The experimental results were fitted

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13

Westenbrink, W. W., J. A. Page, and G. W. VanLoon. "The voltammetric determination of cobalt(II) in seawater – adsorptive preconcentration of the dimethylglyoxime complex." Canadian Journal of Chemistry 68, no. 2 (1990): 209–13. http://dx.doi.org/10.1139/v90-027.

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Conditions for the determination of trace Co in seawater are described. The method involves formation of the dimethylglyoxime complex and adsorptive accumulation onto a hanging mercury drop electrode at an applied potential of −0.70 or −0.96 V vs. SCE. The adsorbed complex is then reduced by scanning the electrode potential to −1.20 V; the reduction peak potential (Ep) is −1.12 V. Nickel behaves in a similar manner with Ep of −0.99 V but the Co complex appears to be preferentially adsorbed, making analysis for Co possible even in the presence of a large excess of Ni. Adsorption of organic matt

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14

Xu, Hongna, Liguo Jin, and Yan Cheng. "Synthesis of Modified Metal Organic Skeleton and Its Adsorption of Hydrochloric Acid Wastewater, Mercury and Arsenic in Water." Science of Advanced Materials 12, no. 7 (2020): 1078–89. http://dx.doi.org/10.1166/sam.2020.3772.

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Metal organic skeleton (MOFs) is a kind of porous material composed of metal ions and organic ligands through coordination, which can be used to absorb a lot of toxic substances from waste water. In this research, UiO-66, UiO-66(Zr) and UiO-66(Zr)–2COOH were synthesized by solvent thermal method, and physical analysis was conducted on the adsorbent properties of the materials by means of XRD, IR, Zeta potential, etc. In the adsorption test of wastewater impurities, UiO-66(Zr)–2COOH was firstly taken as the research object. With the increase of the initial concentration of hydrochloric acid, th

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15

Kim, Yun Sung, Kil Ho Moon, and Jun Heok Lim. "Surface Fractals and Wetting Properties of Porous Anodes Strengthened by Ni₃Al for Molten Carbonate Fuel Cell." Advanced Materials Research 26-28 (October 2007): 861–64. http://dx.doi.org/10.4028/www.scientific.net/amr.26-28.861.

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The contact angles of pure Ni, Ni/7wt%Ni3Al, Ni/5wt%Ni3Al/ 5wt%Cr and Ni/10wt%Cr anodes for the MCFC were measured by means of the capillary rise method in 62mol%Li2CO3+ 38mol%K2CO3 and 52mol%Li2CO3+ 48mol% Na2CO3 electrolyte and at different atmosphere. Also surface fractal dimension (Ds), which could characterize pore structure of the anodes, was calculated from experimental data obtained by mercury porosimetry and nitrogen adsorption method. The surface fractal dimensions of the anode were in range from 2.75 to 2.81, because porosities of the anodes for MCFC were controlled regularly to abo

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16

Srikhaow, Assadawoot, Teera Butburee, Weeraphat Pon-On, et al. "Efficient Mercury Removal at Ultralow Metal Concentrations by Cysteine Functionalized Carbon-Coated Magnetite." Applied Sciences 10, no. 22 (2020): 8262. http://dx.doi.org/10.3390/app10228262.

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This work reports the preparation and utility of cysteine-functionalized carbon-coated Fe3O4 materials (Cys-C@Fe3O4) as efficient sorbents for remediation of Hg(II)-contaminated water. Efficient removal (90%) of Hg(II) from 1000 ppb aqueous solutions is possible, at very low Cys-C@Fe3O4 sorbent loadings (0.01 g sorbent per liter of Hg(II) solution). At low metal concentrations (5–100 ppb Hg(II)), where adsorption is typically slow, Hg(II) removal efficiencies of 94–99.4% were achievable, resulting in final Hg(II) levels of <1.0 ppb. From adsorption isotherms, the Hg(II) adsorption capacity

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17

Balazs, G. Bryan, and Fred C. Anson. "The adsorption of Ni(cyclam)+ at mercury electrodes and its relation to the electrocatalytic reduction of CO2." Journal of Electroanalytical Chemistry 322, no. 1-2 (1992): 325–45. http://dx.doi.org/10.1016/0022-0728(92)80086-j.

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18

Helal, Aasif, Muhammed Naeem, Mohammed Fettouhi, and Md Hasan Zahir. "Fluorescein Hydrazide-Appended Metal–Organic Framework as a Chromogenic and Fluorogenic Chemosensor for Mercury Ions." Molecules 26, no. 19 (2021): 5773. http://dx.doi.org/10.3390/molecules26195773.

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In this work, we prepared a fluorescein hydrazide-appended Ni(MOF) (Metal–Organic Framework) [Ni3(BTC)2(H2O)3]·(DMF)3(H2O)3 composite, FH@Ni(MOF). This composite was well-characterized by PXRD (powder X-ray diffraction), FT-IR (Fourier transform infrared spectroscopy), N2 adsorption isotherm, TGA (thermogravimetric analysis), XPS (X-ray photoelectron spectroscopy), and FESEM (field emission scanning electron microscopy). This composite was then tested with different heavy metals and was found to act as a highly selective and sensitive optical sensor for the Hg2+ ion. It was found that the aque

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19

Zeng, Qiang, Caiting Li, Shanhong Li, et al. "Adsorption and oxidation of elemental mercury from coal-fired flue gas over activated coke loaded with Mn–Ni oxides." Environmental Science and Pollution Research 26, no. 15 (2019): 15420–35. http://dx.doi.org/10.1007/s11356-019-04864-1.

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20

Wang, Zhen, Jing Liu, Yingju Yang, Yingni Yu, Xuchen Yan, and Zhen Zhang. "AMn2O4 (A=Cu, Ni and Zn) sorbents coupling high adsorption and regeneration performance for elemental mercury removal from syngas." Journal of Hazardous Materials 388 (April 2020): 121738. http://dx.doi.org/10.1016/j.jhazmat.2019.121738.

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21

Padilla, Víctor, Núria Serrano, and José Manuel Díaz-Cruz. "Determination of Trace Levels of Nickel(II) by Adsorptive Stripping Voltammetry Using a Disposable and Low-Cost Carbon Screen-Printed Electrode." Chemosensors 9, no. 5 (2021): 94. http://dx.doi.org/10.3390/chemosensors9050094.

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A commercial and disposable screen-printed carbon electrode (SPCE) has been proposed for a fast, simple and low-cost determination of Ni(II) at very low concentration levels by differential pulse adsorptive stripping voltammetry (DPAdSV) in the presence of dimethylglyoxime (DMG) as complexing agent. In contrast with previously proposed methods, the Ni(II)-DMG complex adsorbs directly on the screen-printed carbon surface, with no need of mercury, bismuth or antimony coatings. Well-defined stripping peaks and a linear dependence of the peak area on the concentration of Ni(II) was achieved in the

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22

Shafei, Gamal M. S. El. "Change of Structural and Adsorption Properties Due to Isomorphous Substitution in Hydrotalcite-like Materials." Adsorption Science & Technology 20, no. 8 (2002): 767–86. http://dx.doi.org/10.1260/026361702321104264.

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Samples of hydrotalcite-like compounds with the general formula [M2+1-xM3+x(OH)2]x+•Ax–•nH2O were prepared via coprecipitation through the addition of NaOH to mixed chloride salt solutions. On maintaining the M2+/M3+ ratio equal to three, it was possible to effect isomorphous substitution. This led to the preparation of different compounds which could be compared to the parent material in which M2+ = Ni and M3+ = Al. Other divalent cations used were Mg2+ and Zn2+ with Cr3+ and Fe3+ being employed as trivalent cations. The ratio between cations of the same charge was unity in all the isomorphou

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23

Mustapha, Moshood Keke, and Joy Chinenye Ewulum. "Seasonal assessment, treatment and removal of heavy metal concentrations in a tropical drinking water reservoir." Ekológia (Bratislava) 35, no. 2 (2016): 103–13. http://dx.doi.org/10.1515/eko-2016-0008.

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AbstractHeavy metals are present in low concentrations in reservoirs, but seasonal anthropogenic activities usually elevate the concentrations to a level that could become a health hazard. The dry season concentrations of cadmium, copper, iron, lead, mercury, nickel and zinc were assessed from three sites for 12 weeks in Oyun reservoir, Offa, Nigeria. Triplicate surface water samples were collected and analysed using atomic absorption spectrophotometry. The trend in the level of concentrations in the three sites is site C > B > A, while the trend in the levels of the concentrations in th

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24

Economou, A., and P. R. Fielden. "Selective determination of Ni(II) and Co(II) by flow injection analysis and adsorptive cathodic stripping voltammetry on a wall jet mercury film electrode." Talanta 46, no. 5 (1998): 1137–46. http://dx.doi.org/10.1016/s0039-9140(97)00381-0.

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25

Higgins, Brian, Marcel Pomerleau, Pamela Randolph, Tim Bauer, Jeff Kolde, and Paul Barilla. "Demonstrated Mercury Reduction for SSI MACT Using Mercury Adsorption Modules." Proceedings of the Water Environment Federation 2014, no. 2 (2014): 1–10. http://dx.doi.org/10.2175/193864714816196547.

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26

He, Ping, Huang Qin, Yi Zhang, Xinyi Zhao, Naichao Chen, and Jiang Wu. "Influence of mercury retention on mercury adsorption of fly ash." Energy 204 (August 2020): 117927. http://dx.doi.org/10.1016/j.energy.2020.117927.

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27

Sarkar, D., M. E. Essington, and K. C. Misra. "Adsorption of Mercury(II) by Kaolinite." Soil Science Society of America Journal 64, no. 6 (2000): 1968–75. http://dx.doi.org/10.2136/sssaj2000.6461968x.

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28

Otani, Yoshio, Chikao Kanaoka, Chiyoki Usui, Saburo Matsui, and Hitoshi Emi. "Adsorption of mercury vapor on particles." Environmental Science & Technology 20, no. 7 (1986): 735–38. http://dx.doi.org/10.1021/es00149a014.

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29

Hadi, Pejman, Ming-Ho To, Chi-Wai Hui, Carol Sze Ki Lin, and Gordon McKay. "Aqueous mercury adsorption by activated carbons." Water Research 73 (April 2015): 37–55. http://dx.doi.org/10.1016/j.watres.2015.01.018.

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30

Eswaran, Sandhya, Harvey G. Stenger, and Zhen Fan. "Gas-Phase Mercury Adsorption Rate Studies." Energy & Fuels 21, no. 2 (2007): 852–57. http://dx.doi.org/10.1021/ef060276d.

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31

FURUBAYASHI, Michitaka, and Yasuhiro KUSANO. "Mercury adsorption characteristics of activated carbon." Proceedings of the Symposium on Environmental Engineering 2019.29 (2019): OS203. http://dx.doi.org/10.1299/jsmeenv.2019.29.os203.

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32

Aoyama, M., K. Seki, and S. Doi. "MERCURY ADSORPTION ONTO PYROLYZED WASTE PAPER." Journal of Environmental Science and Health, Part A 36, no. 10 (2001): 2047–54. http://dx.doi.org/10.1081/ese-100107447.

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33

Daza, L. "Mercury Adsorption by Sulfurized Fibrous Silicates." Clays and Clay Minerals 39, no. 1 (1991): 14–21. http://dx.doi.org/10.1346/ccmn.1991.0390102.

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34

Komorsky-Lovrić, Šebojka, and Milivoj Lovrić. "Berberine adsorption at a mercury electrode." Mikrochimica Acta 97, no. 3-4 (1989): 159–69. http://dx.doi.org/10.1007/bf01242462.

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35

Jin, Wenrui, and Jixian Peng. "Adsorption voltammetry at a mercury ultramicroelectrode." Journal of Electroanalytical Chemistry 345, no. 1-2 (1993): 433–44. http://dx.doi.org/10.1016/0022-0728(93)80494-3.

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36

Coats, A. M., E. Cooper, and R. Raval. "Toluene adsorption on Ni(111)." Surface Science 307-309 (April 1994): 89–94. http://dx.doi.org/10.1016/0039-6028(94)90375-1.

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37

Jones, Robert G., and Nagindar K. Singh. "CF3I adsorption on Ni{100}." Vacuum 38, no. 4-5 (1988): 213–18. http://dx.doi.org/10.1016/0042-207x(88)90047-4.

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38

Klink, C., M. Foss, I. Stensgaard, and F. Besenbacher. "Bi adsorption on Ni(100)." Surface Science Letters 251-252 (July 1991): A362. http://dx.doi.org/10.1016/0167-2584(91)90981-v.

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39

Benndorf, Carsten, and Lutz Meyer. "CO adsorption on Ni(551)." Surface Science Letters 251-252 (July 1991): A364. http://dx.doi.org/10.1016/0167-2584(91)90987-3.

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40

Benndorf, Carsten, and Lutz Meyer. "CO adsorption on Ni(551)." Surface Science 251-252 (July 1991): 872–76. http://dx.doi.org/10.1016/0039-6028(91)91115-e.

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41

Klink, C., M. Foss, I. Stensgaard, and F. Besenbacher. "Bi adsorption on Ni(100)." Surface Science 251-252 (July 1991): 841–45. http://dx.doi.org/10.1016/0039-6028(91)91109-b.

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42

Watson, Charles M., Daniel J. Dwyer, Jeffrey C. Andle, Alice E. Bruce, and Mitchell R. M. Bruce. "Stripping Analyses of Mercury Using Gold Electrodes: Irreversible Adsorption of Mercury." Analytical Chemistry 71, no. 15 (1999): 3181–86. http://dx.doi.org/10.1021/ac981312b.

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43

Yan, Tsoung Y. "Mercury Removal from Oil by Reactive Adsorption." Industrial & Engineering Chemistry Research 35, no. 10 (1996): 3697–701. http://dx.doi.org/10.1021/ie950630n.

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44

Karata, Despina, Amedeo Lancia, Dino Musmarra, and Francesco Pepe. "Adsorption of metallic mercury on activated carbon." Symposium (International) on Combustion 26, no. 2 (1996): 2439–45. http://dx.doi.org/10.1016/s0082-0784(96)80074-9.

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45

Liao, Lixia, H. M. Selim, and R. D. DeLaune. "Mercury Adsorption-Desorption and Transport in Soils." Journal of Environmental Quality 38, no. 4 (2009): 1608–16. http://dx.doi.org/10.2134/jeq2008.0343.

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46

Kiekens, P., F. Den Van Broecke, M. Bogaert, and E. Temmerman. "Underpotential Adsorption of Mercury on Glassy Carbon." Bulletin des Sociétés Chimiques Belges 92, no. 11-12 (2010): 929–34. http://dx.doi.org/10.1002/bscb.19830921103.

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47

Viraraghavan, T., and A. Kapoor. "Adsorption of mercury from wastewater by peat." Journal of Environmental Science and Health . Part A: Environmental Science and Engineering and Toxicology 30, no. 3 (1995): 553–66. http://dx.doi.org/10.1080/10934529509376217.

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48

Wang, Yeh-Sheng, Chih-Chia Cheng, Jem-Kun Chen, Fu-Hsiang Ko, and Feng-Chih Chang. "Bioinspired supramolecular fibers for mercury ion adsorption." Journal of Materials Chemistry A 1, no. 26 (2013): 7745. http://dx.doi.org/10.1039/c3ta11072a.

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49

Sieńko, Dorota, Jolanta Nieszporek, Krzysztof Nieszporek, Dorota Gugała, and Jadwiga Saba. "Adsorption of Cytosine on a Mercury Electrode." Collection of Czechoslovak Chemical Communications 71, no. 10 (2006): 1393–406. http://dx.doi.org/10.1135/cccc20061393.

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The electrosorption behavior of cytosine at the mercury electrode/acetic buffer of pH 4 and 5 interfaces was determined from the double-layer differential capacity measurements extrapolated to zero frequency. Solutions of cytosine were prepared to cover the range from 1 × 10-4 to 6 × 10-3 mol dm-3. Adsorption of cytosine was described by the adsorption isotherms constants derived from the surface pressure data as a function of electrode charge density and bulk concentration. The obtained values of the relative surface excesses Γ′ were higher in the acetic buffer of pH 4 than of pH 5. Maximum o

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50

Monterrozo, Rodolfo Abraham, Maohong Fan, and Morris D. Argyle. "Adsorption of Mercury with Modified Thief Carbons." Journal of Environmental Engineering 138, no. 3 (2012): 386–91. http://dx.doi.org/10.1061/(asce)ee.1943-7870.0000434.

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