Yantasee, Wassana; Lin, Yuehe; Fryxell, Glen E.; Busche, Brad J.; Birnbaum, Jerome C.
Pacific Northwest National Lab., Richland, WA (United States). Funding organisation: US Department of Energy (United States)2003
Pacific Northwest National Lab., Richland, WA (United States). Funding organisation: US Department of Energy (United States)2003
AbstractAbstract
[en] Self-assembled monolayers of carbamoylphosphonic acids (acetamide phosphonic acid and propionamide phosphonic acid) on mesoporous silica supports were studied as potential absorbents for heavy and transition metal ions in aqueous wastes. The adsorption capacity, selectivity, and kinetics of the materials in sequestering metal ions, including Cd2+, Co2+, Cu2+, Cr3+, Pb2+, Ni2+, Zn2+, and Mn2+, were measured in batch experiments with excess sodium ion. The solution pH ranged from 2.2 to 5.5. The kinetics study shows that the adsorption reached equilibrium in seconds, indicating that there is little resistance to mass transfer, intraparticle diffusion, and surface chemical reaction. The competitive adsorption study found the phosphonic acid-SAMMS to have an affinity for divalent metal ions in decreasing order of Pb2+ > Cu2+ > Mn2+ > Cd2+ > Zn2+ > Co2+ > Ni2+. The measured Cd2+ adsorption isotherm was of the Langmuirian type and had a saturation binding capacity of 0.32 mmol/g
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PNNL-SA--38412; 400403209; AC06-76RL01830
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Matyas, Josef; Fryxell, Glen E.; Busche, Brad J.; Wallace, Krys; Fifield, Leonard S.
Pacific Northwest National Laboratory, Richland, WA (United States). Funding organisation: US Department of Energy (United States)2011
Pacific Northwest National Laboratory, Richland, WA (United States). Funding organisation: US Department of Energy (United States)2011
AbstractAbstract
[en] To support the future expansion of nuclear energy, an effective method is needed to capture and safely store radiological iodine-129 released during reprocessing of spent nuclear fuel. Various materials have been investigated to capture and immobilize iodine. In most cases, however, the materials that are effective for capturing iodine cannot subsequently be sintered/densified to create a stable composite that could be a viable waste form. We have developed chemically modified, highly porous, silica aerogels that show sorption capacities higher than 440 mg of I2 per gram at 150 C. An iodine uptake test in dry air containing 4.2 ppm of iodine demonstrated no breakthrough after 3.5 h and indicated a decontamination factor in excess of 310. Preliminary densification tests showed that the I2-loaded aerogels retained more than 92 wt% of I2 after thermal sintering with pressure assistance at 1200 C for 30 min. These high capture and retention efficiencies for I2 can be further improved by optimizing the functionalization process and the chemistry as well as the sintering conditions.
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16 Nov 2011; vp; Ceramic Materials for Energy Applications: American Ceramic Society's 35th International Conference on Advanced Ceramics and Composites; Daytona Beach, FL (United States); 23-28 Jan 2011; AF5805000; AC05-76RL01830; Available from Wiley, Hoboken, NJ (US); Ceramic Engineering and Science Proceedings, Y Katoh, et al; 32(9):23-33; doi 10.1002/9781118095386.ch3
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BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, CLEANING, ELEMENTS, ENERGY, ENERGY SOURCES, FABRICATION, FLUIDS, FUELS, GASES, HALOGENS, INTERMEDIATE MASS NUCLEI, INTERNAL CONVERSION RADIOISOTOPES, IODINE ISOTOPES, ISOTOPES, MATERIALS, MINERALS, NONMETALS, NUCLEI, ODD-EVEN NUCLEI, OXIDE MINERALS, RADIOACTIVE MATERIALS, RADIOACTIVE WASTES, RADIOISOTOPES, REACTOR MATERIALS, SEPARATION PROCESSES, WASTES, YEARS LIVING RADIOISOTOPES
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AbstractAbstract
[en] A new sensor was developed for simultaneous detection of cadmium (Cd2+), copper (Cu2+), and lead (Pb2+), based on the voltammetric response at a carbon paste electrode modified with carbamoylphosphonic acid (acetamide phosphonic acid) self-assembled monolayer (SAM) on mesoporous silica (Ac-Phos SAMMS). The adsorptive stripping voltammetry (AdSV) technique involves preconcentration of the metal ions onto Ac-Phos SAMMS under an open circuit, then electrolysis of the preconcentrated species, followed by a square wave potential sweep towards positive values. Factors affecting the preconcentration process were investigated. The voltammetric responses increased linearly with the preconcentration time from 1 to 30 min or with metal ion concentrations ranging from 10 to 200 ppb. The responses also evolved in the same fashion as adsorption isotherm in the pH range of 2-6. The metal detection limits were 10 ppb after 2 min preconcentration and improved to 0.5 ppb after 20 min preconcentration
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S0003267003013126; Copyright (c) 2003 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)
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Birnbaum, Jerome C.; Busche, Brad J.; Lin, Yuehe; Shaw, Wendy J.; Fryxell, Glen E.
Pacific Northwest National Lab., Richland, WA (United States). Funding organisation: US Department of Energy (United States)2001
Pacific Northwest National Lab., Richland, WA (United States). Funding organisation: US Department of Energy (United States)2001
AbstractAbstract
[en] The synthesis of carbamoylphosphonate silanes (CMPO analogs) designed for sequestering actinide cations in self-assembled monolayers on mesoporous supports (SAMMS) is described
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PNNL-SA--36185; EW4090100; AC06-76RL01830
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Journal Article
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Journal of the Chemical Society. Chemical Communications; ISSN 0009-241X; ; v. 13; p. 1374-1375
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