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Relevant bibliographies by topics / Platinum group analytical chemistry

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Academic literature on the topic 'Platinum group analytical chemistry'

Author: Grafiati

Published: 4 June 2021

Last updated: 8 February 2022

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Journal articles on the topic "Platinum group analytical chemistry"

1

Brajter, Krystyna, Krystyna Slonawska, and James A. Cox. "Separation of platinum group metal ions by Donnan dialysis." Analytical Chemistry 57, no. 12 (October 1985): 2403–5. http://dx.doi.org/10.1021/ac00289a055.

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GAGNON, ZOFIA E., CATHERINE NEWKIRK, and STEVEN HICKS. "Impact of Platinum Group Metals on the Environment: A Toxicological, Genotoxic and Analytical Chemistry Study." Journal of Environmental Science and Health, Part A 41, no. 3 (March 2006): 397–414. http://dx.doi.org/10.1080/10934520500423592.

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Myasoedova, G. V., E. A. Zaharchenko, O. B. Mokhodoeva, I. V. Kubrakova, and V. A. Nikashina. "Sorption Preconcentration of Platinum-Group Metals with Filled Fibrous POLYORGS Sorbents." Journal of Analytical Chemistry 59, no. 6 (June 2004): 536–40. http://dx.doi.org/10.1023/b:janc.0000030873.88087.f0.

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Moldovan, Mariella. "Origin and fate of platinum group elements in the environment." Analytical and Bioanalytical Chemistry 388, no. 3 (March 13, 2007): 537–40. http://dx.doi.org/10.1007/s00216-007-1234-y.

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Schuster, M., D. Hollmann, and K. H. König. "On the analysis of platinum group metals." Fresenius' Zeitschrift für analytische Chemie 333, no. 7 (January 1989): 780. http://dx.doi.org/10.1007/bf00476636.

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Volynskii, A. B. "Chemical Modifiers Based on Platinum-Group Metal Compounds in Electrothermal Atomic Absorption Spectrometry." Journal of Analytical Chemistry 59, no. 6 (June 2004): 502–20. http://dx.doi.org/10.1023/b:janc.0000030869.61576.d9.

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Petrucci, Francesco, Nicola Violante, Oreste Senofonte, Marco De Gregorio, Alessandro Alimonti, Sergio Caroli, Giovanni Forte, and Antonio Cristaudo. "Development of an analytical method for monitoring worker populations exposed to platinum-group elements." Microchemical Journal 76, no. 1-2 (February 2004): 131–40. http://dx.doi.org/10.1016/j.microc.2003.11.005.

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Rao, C. R. M., and G. S. Reddi. "Platinum group metals (PGM); occurrence, use and recent trends in their determination." TrAC Trends in Analytical Chemistry 19, no. 9 (September 2000): 565–86. http://dx.doi.org/10.1016/s0165-9936(00)00031-5.

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Locatelli, Clinio. "Voltammetric Analysis of Trace Levels of Platinum Group Metals – Principles and Applications." Electroanalysis 19, no. 21 (November 2007): 2167–75. http://dx.doi.org/10.1002/elan.200704026.

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Wang, Hao, and Di-Jia Liu. "Rational design of platinum-group-metal-free electrocatalysts for oxygen reduction reaction." Current Opinion in Electrochemistry 28 (August 2021): 100724. http://dx.doi.org/10.1016/j.coelec.2021.100724.

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Dissertations / Theses on the topic "Platinum group analytical chemistry"

1

Schmidt, Lilian Olga. "Aspects of the determination of the platinum group elements and arsenic by inductively coupled plasma mass spectrometry." Thesis, Pretoria : [s.n.], 2001. http://upetd.up.ac.za/thesis/available/etd-02242006-123310/.

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Surakitbanharn, Yosyong. "The efficient separation of platinum group metals using centrifugal partition chromatography." Diss., The University of Arizona, 1992. http://hdl.handle.net/10150/186074.

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Centrifugal Partition Chromatography (CPC) is a multistage liquid-liquid countercurrent distribution technique which utilizes rotating teflon cartridges to hold a liquid phase stationary while the other liquid phase is pumped at a constant flow rate. It has been demonstrated to be a valuable technique for the base line separations of families of metal ions such as the platinum group metals (PGM)--Pt, Pd, Rh and Ir. The separations of these metals as their anionic chloro complexes were achieved using the heptane-water phase pair with a stable and relatively inexpensive extractant trioctylphosphine oxide (TOPO) functioning as a ligand in its neutral form and as a cation in its protonated form. A striking feature of the chromatograms of the complexes and ion pairs were their much poorer efficiencies compared to the efficiency of an organic analyte like 3-picoline under identical distribution rations. The inefficiencies of the PGM separations were also a function of the concentrations of the aqueous and organic phase components. These inefficiencies could be attributed to slow kinetics of the back extraction of the complexes and ion pairs and could be used to derive the mechanisms of these slow chemical kinetic steps. A correlation was established for the Pd(II) system between the CPC inefficiencies and the half lives of the slow reactions measured independently by stopped flow in micelles. This correlation was utilized to derive the rate constants for the back extraction of the TOPO complexes and ion pairs of Pt and Ir. The mechanisms of the extraction reactions were derived using the principle of microscopic reversibility based on the mechanisms of the back extraction reactions. This was then used to obtain estimates for the rate constants for the extraction reactions as well. The PGM were thus separated and their equilibrium and kinetics (extraction and back extraction) completely characterized using CPC. This is a significant development with CPC because such complete equilibrium and kinetic characterizations are hard to achieve with conventional liquid chromatographic techniques.

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Alshana, Usama Ahmed. "Separation And Quantitation Of Some Platinum Group Metals By Rp-hplc." Master's thesis, METU, 2005. http://etd.lib.metu.edu.tr/upload/3/12605760/index.pdf.

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In this study, a reversed-phase high performance liquid chromatography (RP-HPLC) method has been developed to separate and determine Pt and Pd after formation of their chelates with N,N-diethyl-N'
-benzoylthiourea (DEBT). With the aim of reducing the number of steps in treating the samples, the method developed does not require the elimination of excess chelating reagent before the analysis of metal chelates. The different physical and chemical parameters affecting separation were examined in details. The whole analysis was completed on a C18 column in 16 min at 280 nm, with the mobile phase of acetonitrile-methanol-water (80:10:10, v:v:v) containing 0.20 mol l-1 pH 5.0 acetate buffer at a flow rate of 0.8 ml min-1. Detection limits of the method, based on 3s, were found as 14.2 ug l-1 for Pd and 0.77 mg l-1 for Pt using a 20-ul sample loop. Reproducibility of the method for ten repeated measurements was found as 2.36 % for 0.60 mg l-1 Pd and 2.58 % for 10.0 mg l-1 Pt as % RSD. The proposed method is a rapid, simple and highly selective method for the simultaneous determination of Pt and Pd by HPLC without the need for any interference elimination process.

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Dorflinger, Charles. "CHARACTERIZATION OF CARBON FIBER MICROELECTRODES DECORATED WITH PLATINUM NANOPARTICLES." Case Western Reserve University School of Graduate Studies / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=case1396887958.

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Scanlan, Thomas Huw. "Platinum group chemistry of iminophosphines and related ligands." Thesis, University of Newcastle Upon Tyne, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.391972.

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Harding, Nigel Anthony. "β-thia-alkyl complexes of platinum group metals." Thesis, Imperial College London, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283721.

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Trenholme, W. J. F. "Metal-organic frameworks for platinum group metal extraction." Thesis, University of Nottingham, 2016. http://eprints.nottingham.ac.uk/32795/.

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This Thesis describes the synthesis and characterisation of a variety of functionalised metal-organic frameworks (MOFs). These MOFs have been used for the extraction of platinum group metal (PGM) compounds from aqueous and organic solvents and for the storage of gases such as CO2, CH4 and the C2 hydrocarbons. Chapter 1 contains an introduction to PGM properties and uses with specific focus on the chemical properties which allow for separation of PGMs from base metal compounds and for separation between different PGM compounds. The synthesis and structure prediction of MOFs is then introduced, leading into an overview of the use of functionalised MOFs, especially those used for the encapsulation and extraction of metal ions from solution. General experimental techniques and details are described, as is the theory behind inductively coupled plasma optical emission spectrometry (ICP-OES), the most widely used analytical technique reported in this work. Chapter 2 describes the synthesis of chemically stable amine-functionalised Zr(IV) MOFs; UiO-68-NH2 and UiO-66-NH2, for extraction of PGM anions from aqueous and acidic solutions. ICP-OES was used to show that both materials exhibit close to 100% uptake of PtCl62- when present in just 3.5 equivalents per anion, comparable to the best materials reported for PtCl62- extraction. Furthermore, UiO-66-NH2 exhibited consistently higher PtCl62- uptake from aqueous solutions than four industrially used materials supplied by Johnson Matthey. Back-extraction of PtCl62- was demonstrated simply by heating the doped MOF in 4 M HCl, removing 99% of the PGM while maintaining the phase and crystallinity of UiO-66-NH2. Separation of PdCl62- from PtCl62- from acidic HCl solutions was exhibited by UiO-66-NH2, showing an exceptional selectivity of 20:1 for Pd:Pt from 2 M HCl. Likewise, 100% selectivity for PtCl62- and PdCl62- over CuCl2 and CuSO4 from acidic solutions was demonstrated, even in cases in which Cu was in 100-fold excess. Solid state NMR was employed to confirm the interaction between the framework and the PGM anions, with XPS results suggesting that the encapsulated Pt species within UiO-66-NH2 may be PtCl3(NH2)3 or PtCl4(NH2)2. Chapter 3 describes the synthesis and characterisation of a series of functionalised Cu(II) MOFs, NOTT-151, -155, -125 and -150, for the removal of neutral PGM complexes, Pd(OAc)2, PtCl4 and Rh2(OAc)4, from THF. The design of the MOFs allowed for an investigation into the effect of different topologies (ssa and fof), cage sizes and functional groups (amine, oxamide and methyl) on the uptake of each PGM complex. ICP-OES analysis showed that the MOFs were capable of extracting each PGM complex. The oxamide-functionalised NOTT-125 exhibited the most consistent uptake of Pd(OAc)2 with a maximum capacity of 35 mg g-1 (7 NH(CO)2NH groups per PtCl4). The amine-functionalised NOTT-155 showed the highest uptake of PtCl4, with a maximum capacity of 73 mg g-1 (4 NH2 groups per PtCl4). Uptake of Rh2(OAc)4 was generally low, however NOTT-125 showed a maximum extraction of 87 mg g-1 (3 NH(CO)2NH groups per PGM). The larger pore fof MOFs, NOTT-155 and NOTT-125, were more effective for each extraction than the MOFs of ssa topology, NOTT-151 and NOTT-150. However, of the ssa MOFs, amine-functionalised NOTT-151 was shown to give higher uptake of each PGM than the isostructural methyl-functionalised NOTT-150. This demonstrated the importance of incorporating a functional group capable of coordinating to the metal complex. Chapter 4 introduces the use of a nitrogen-rich triazine core in the synthesis of a variety of organic linkers to prepare MOFs for gas storage applications. The preparation of a novel 3,24-connected Cu(II) MOF of rht topology, denoted NOTT-160, is described and the structure characterised using X-ray crystallography. The material is shown to exhibit good uptake of C2 hydrocarbons with uptake of 128 cc g-1, 115 cc g-1, 110 cc g-1 for C2H2, C2H4, C2H6 respectively at 298 K and 1 bar (this becomes 212 cc g-1, 175 cc g-1 and 201 cc g-1 at 273 K and 1 bar). The selectivities of 79:1 and 70:1 calculated using Henry’s law for the separations of C2H2:CH4 and C2H4:CH4 respectively at 298 K are the third and second highest reported values for a MOF under these conditions. Ideal adsorbed solution theory (IAST) was also employed to calculate and predict these selectivities and shows agreement with the results obtained using Henry’s law. In addition, NOTT-160 shows an exceptional volumetric working capacity for CH4 of 221 cm3 cm-3 at 80 bar and 298 K. This is the second highest working capacity reported for a MOF under these conditions, with the excellent performance attributed to the high porosity and comparatively high crystal density of the material. Chapter 5 contains a summary of the work presented in this thesis.

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Auer, Derek. "Flow-injection analysis of the platinum-group metals." Doctoral thesis, University of Cape Town, 1995. http://hdl.handle.net/11427/17511.

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Includes bibliographical references.
To date the principle methods for the determination of the platinum-group metals (PGMs) use an "off-line" assay with flame-atomic absorption spectrometry and visible spectrometry. Both suffer numerous interferences and involve time-consuming and arduous laboratory separation methods prior to analysis. An "on-line" method for the rapid assay of the PGMs is indeed a lacking component in the analysts' repertoire of methods. This study describes the development of spectrophotometric methods for the determination of the PGMs using flow-injection analysis (FIA). The principle of exploiting the remarkably specific and selective reaction of stannous halides with the PGMs to yield a series of intensely coloured complexes in acidic solutions forms the basis of these methods. The reaction is subject to relatively few interferences from other transition metals. A high speed scanning spectrophotometer is employed to obtain second order data. The successful manipulation of the data enables the determination of PGMs as single components and also simultaneously in mixtures. Attention is focused on the establishment of principles for successful multi-component analysis of PGMs. The development of a software program for multi-wavelength data manipulation was mandatory and is described. Criteria for successful selection of analytical wavelengths are discussed. The usefulness of multi-dimensional graphical data representation is demonstrated in a stop-flow study of the palladium reaction with tin (II) chloride. Qualitative information is provided regarding the nature of complexes and their interactions. Correlation of spectrophotometric data with complex solution colour changes is made. The requirements for future progress in multi-component FIA determinations as well as the direction for future research conclude the study.

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Arnold, Philip M. "Coordination chemistry of platinum group metals with sulphur-containing ligands." Thesis, University of Oxford, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.249298.

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Wenger, J. C. "Surface chemistry of the group IIB metal dimethyls on platinum." Thesis, University of East Anglia, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334697.

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Books on the topic "Platinum group analytical chemistry"

1

Wenger, John Charles. Surface chemistry of the group IIB metal dimethyls on platinum. Norwich: University of East Anglia, 1993.

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Lustig, Sönnke. Platinum in the environment: Car catalyst emitted platinum ; transformation behaviour in soil and platinum accumulation in plants : speciation investigations. München: Utz, 1997.

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3

Jaffé, Hans H. Symmetry in chemistry. Mineola, N.Y: Dover Publications, 2002.

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4

Hartley, F. R. Chemistry of the Platinum Group Metals: Recent Developments (Studies in Inorganic Chemistry). Elsevier Science, 1991.

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R, Hartley F., ed. Chemistry of the platinum group metals: Recent developments. Amsterdam: Elsevier, 1991.

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Chemistry of the Platinum Group Metals - Recent Developments. Elsevier, 1991. http://dx.doi.org/10.1016/c2009-0-08900-4.

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Nuclear Analytical Methods for Platinum Group Elements (Iaea Tecdoc Series). International Atomic Energy Agency, 2005.

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Xie Gao YangYu Lian MinLiu Ben YaoShen Pan Wen. Manganese Sub-group Elements, Iron and Platinum / inorganic chemistry series /Chinese classics of science and technology. Science Press, 1996.

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9

C, Bruneau, and Dixneuf P. H, eds. Ruthenium catalysts and fine chemistry. Berlin: Springer, 2004.

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Orchin, Milton, and Hans H. Jaffe. Symmetry in Chemistry. Dover Publications, 2002.

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Book chapters on the topic "Platinum group analytical chemistry"

1

Barea, Elisa, L. Marleny Rodríguez-Albelo, and Jorge A. R. Navarro. "Platinum Group Metal-Organic Frameworks." In The Chemistry of Metal-Organic Frameworks: Synthesis, Characterization, and Applications, 203–30. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527693078.ch8.

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Schetinger, Maria Rosa Chitolina, Vera Maria Morsch, and Denise Bohrer. "Aluminum: Interaction with Nucleotides and Nucleotidases and Analytical Aspects of Its Determination." In Group 13 Chemistry II, 99–137. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-45425-x_4.

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Haynes, L. "Platinum-Group Element Chemistry in Relation to the Behaviour of Individual PGEs in Primary and Secondary Geological Processes." In Geo-Platinum 87, 407. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1353-0_42.

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Cantale, C., M. Casarci, A. De Stefanis, G. M. Gasparini, L. Nardi, and A. Salluzzo. "N,N Dialkylaliphatic Amides as Extractant of Platinum Group Metals." In New Separation Chemistry Techniques for Radioactive Waste and Other Specific Applications, 57–63. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3654-9_10.

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Griffiths, C. M., W. M. Thomas, and W. Pope. "Sampling and Analytical Techniques and their Application to Soil Chemistry, Hydrogeology and Hydrochemistry in Group Condition Surveys." In Contaminated Soil, 399–401. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-5181-5_44.

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Izatt, Steven R., James S. McKenzie, Ronald L. Bruening, Reed M. Izatt, Neil E. Izatt, and Krzysztof E. Krakowiak. "Selective Recovery of Platinum Group Metals and Rare Earth Metals from Complex Matrices Using a Green Chemistry/Molecular Recognition Technology Approach." In Metal Sustainability, 317–32. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119009115.ch14.

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Khoo, S. B., and B. T. Tay. "UTILIZATION OF PLATINUM THIN RING ELECTRODES AS HPLC DETECTOR AND IN ANODIC STRIPPING VOLTAMMETRY." In Analytical Chemistry, 298–317. WORLD SCIENTIFIC, 1990. http://dx.doi.org/10.1142/9789814434508_0026.

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Van Loon, J. C., and R. R. Barefoot. "Determination of the Platinum Group Metals and Gold." In Analytical Methods for Geochemical Exploration, 251–91. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-12-714170-1.50011-6.

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Balko, E. N. "Electrochemical Applications of the Platinum Group Metals: Platinum Group Metal Coated Anodes." In Chemistry of the Platinum Group Metals - Recent Developments, 267–301. Elsevier, 1991. http://dx.doi.org/10.1016/b978-0-444-88189-2.50015-8.

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Knifton, J. F. "Platinum Group Catalysis in Melts." In Chemistry of the Platinum Group Metals - Recent Developments, 124–46. Elsevier, 1991. http://dx.doi.org/10.1016/b978-0-444-88189-2.50011-0.

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Conference papers on the topic "Platinum group analytical chemistry"

1

Bernal, José, Ana María Ares, Jorge Bernal, María Jesús Nozal, and Francisco Javier Sánchez. "Results of the use of Kahoot! gamification tool in a course of Chemistry." In Fourth International Conference on Higher Education Advances. Valencia: Universitat Politècnica València, 2018. http://dx.doi.org/10.4995/head18.2018.8179.

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The present study examines the use of Kahoot! as a gamification tool to explore mixed learning strategies. We analyze its use in two different groups of a theoretical subject of the third course of the Degree in Chemistry. An empirical-analytical methodology was used using Kahoot! in two different groups of students, with different frequencies. The academic results of these two group of students were compared between them and with those obtained in the previous course, in which Kahoot! was not employed, with the aim of measuring the evolution in the students´ knowledge. The results showed, in all cases, that the use of Kahoot! has led to a significant increase in the overall marks, and in the number of students who passed the subject. Moreover, some differences were also observed in students´ academic performance according to the group. Finally, it can be concluded that the use of a gamification tool (Kahoot!) in a university classroom had generally improved students´ learning and marks, and that this improvement is more prevalent in those students who have achieved a better Kahoot! performance.

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Aoyagi, Mitsuhiro, Akihiro Uchibori, Takahi Takata, David L. Y. Louie, and Andrew J. Clark. "Sodium Fire Analysis Using a Sodium Chemistry Package in MELCOR." In 2020 International Conference on Nuclear Engineering collocated with the ASME 2020 Power Conference. American Society of Mechanical Engineers, 2020. http://dx.doi.org/10.1115/icone2020-16751.

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Abstract The Sodium Chemistry (NAC) package in MELCOR has been developed to enhance application to sodium cooled fast reactors. The models in the NAC package have been assessed through benchmark analyses. The F7-1 pool fire experimental analysis is conducted within the framework of the U.S.–Japan collaboration; Civil Nuclear Energy Research and Development Working Group. This study assesses the capability of the pool fire model in MELCOR and provides recommendations for future model improvements because the physics of sodium pool fire are complex. Based on the preliminary results, analytical conditions, such as heat transfer on the floor catch pan are modified. The current MELCOR analysis yields lower values than the experimental data in pool combustion rate and pool, catch pan, and gas temperature during early time. The current treatment of heat transfer for the catch pan is the primary cause of the difference in the results from the experimental data. After sodium discharge stopping, the pool combustion rate and temperature become higher than experimental data. This is caused by absence of a model for pool fire suppression due to the oxide layer buildup on the pool surface. Based on these results, recommendations for future works are needed, such as heat transfer modification in terms of the catch pan and consideration of the effects of the oxide layer for both the MELCOR input model and pool physic.

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Baniya, A., S. Thapa, E. Borquist, D. Bailey, D. Wood, G. Dutta, P. Arumugam, J. Glawe, C. Kevil, and L. Weiss. "Lab-on-a-Chip Device for Hydrogen Sulfide Sensing in Biomedical and Environmental Applications Using Electrochemical Approach." In ASME 2015 International Technical Conference and Exhibition on Packaging and Integration of Electronic and Photonic Microsystems collocated with the ASME 2015 13th International Conference on Nanochannels, Microchannels, and Minichannels. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/ipack2015-48491.

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Hydrogen sulfide (H2S) is rapidly emerging as a biologically significant signaling molecule. In recent studies, sulfide level in blood or plasma has been reported to be in the concentration between 10 and 300 μM suggesting it acts in various diseases. This work reports progress on a new Lab-on-a-Chip (LOC) device for these applications. The uniquely designed, hand-held device uses advanced liberation chemistry that releases H2S from liquid sample and an electrochemical approach to detect sulfide concentration from the aqueous solution. The device itself consists of three distinct layers of Polydimethylsiloxane (PDMS) structures and a three electrode system for direct and rapid H2S concentration measurement. In this work specifically, the oxidation of sulfide at the gold (Au) and platinum (Pt.) electrodes has been examined. This is the first known application of electrochemical H2S sensing in an LOC application. The analytical utility and performance of the device has been assessed through direct detection using chronoamperometry (CA) scan and cyclic voltammetry (CV). An electrocatalytic sulfide oxidation signal has been recorded for sulfide concentration range vs, Ag/AgCl at different pH buffers at the trapping chamber. The calibration curve in the range 1 μM to 1 M was obtained using this electrode setup. The detection limit was found to be 0.1 μM. This device shows promise for providing fast and inexpensive determination of H2S concentration in aqueous samples.

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Balkey, J. J., R. L. Dodge, B. T. Martinez, and R. E. Wieneke. "Data Collection and Tracking of Radioactive Waste at the Los Alamos National Laboratory Plutonium Facility." In ASME 2003 9th International Conference on Radioactive Waste Management and Environmental Remediation. ASMEDC, 2003. http://dx.doi.org/10.1115/icem2003-4586.

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The Los Alamos National Laboratory (LANL) is one of two design laboratories in the United States Department of Energy’s weapons complex, with over 60 years of experience in handling radioactive materials, and, consequently, in managing radioactive waste. Actinide research and development is conducted at the Plutonium Facility, which has been in operation since 1978 and is the major source of radioactive waste at LANL. The Nuclear Materials Technology (NMT) Division is responsible for operating the Plutonium Facility and has a dedicated group of personnel who manage radioactive and hazardous waste, and address environmental regulations. The NMT Division also oversees analytical support operations in the Chemistry and Metallurgy Research Facility. Operations at these two nonreactor nuclear facilities generate a wide variety of waste that may be generally classified as sanitary, hazardous, radioactive, and mixed (both radioactive and hazardous). The expedient, cost-effective, and regulatory-compliant management of radioactive waste has been a challenging task, given the propensity for rapid change in the regulatory environment. One major asset is the availability of information on waste generation and characteristics in electronic form. To do so, the Waste Inventory Tracking system (WITS) was developed 6 years ago to collect and store this information. To record waste information in the field, technicians use handheld Palm Pilots®. These units are then docked with personal computers to transfer the data to WITS. The primary use of WITS is the automated generation of waste package data reports, which are used to demonstrate compliance with waste acceptance criteria and gain acceptance for waste disposal. The WITS data are also used to evaluate various aspects of waste generation and handling, and to track performance indicators. The WITS is a fundamental part of waste management in the NMT Division.

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Reports on the topic "Platinum group analytical chemistry"

1

Eisenberg, R. Photochemistry and charge transfer chemistry of the platinum group elements. Office of Scientific and Technical Information (OSTI), December 1992. http://dx.doi.org/10.2172/6673318.

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Eisenberg, R. Photochemistry and charge transfer chemistry of the platinum group elements. Office of Scientific and Technical Information (OSTI), December 1991. http://dx.doi.org/10.2172/5713717.

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Eisenberg, R. Photochemistry and charge transfer chemistry of the platinum group elements. Progress report, May 1, 1991--April 30, 1992. Office of Scientific and Technical Information (OSTI), December 1991. http://dx.doi.org/10.2172/10121488.

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Eisenberg, R. Photochemistry and charge transfer chemistry of the platinum group elements. Summary progress report, May 1, 1990--April 30, 1993. Office of Scientific and Technical Information (OSTI), December 1992. http://dx.doi.org/10.2172/10142611.

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Stanley, Floyd E., Khalil J. Spencer, Kevin J. Kuhn, and Lav Tandon. Design and Application of TIMS-Based Thorium Measurement Methods in the Actinide Analytical Chemistry Group at Los Alamos National Laboratory. Office of Scientific and Technical Information (OSTI), January 2013. http://dx.doi.org/10.2172/1059403.

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Ames, D. E., and G. Tuba. Epidote-amphibole and accessory phase mineral chemistry as a vector to low-sulphide platinum group element mineralization, Sudbury: laser ablation ICP-MS trace element study of hydrothermal alteration. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2015. http://dx.doi.org/10.4095/296695.

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