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Skrzypczak, A.
Funding organisation: Polish Committee of Scientific Research (Poland)
Proceedings of the 22. International Symposium on Physico-Chemical Methods of Separation - Ars Separatoria 20072007
Funding organisation: Polish Committee of Scientific Research (Poland)
Proceedings of the 22. International Symposium on Physico-Chemical Methods of Separation - Ars Separatoria 20072007
AbstractAbstract
No abstract available
Primary Subject
Source
Trochimczuk, A.W.; Walkowiak, W. (eds.); Wroclaw University of Technology, Wroclaw (Poland); Nicolaus Copernicus University, Torun (Poland); 217 p; ISBN 978-83-7493-317-9;
; 2007; p. 181; 22. International Symposium on Physico-Chemical Methods of Separation - Ars Separatoria 2007; Szklarska Poreba (Poland); 10-14 Jun 2007; Also available from Wroclaw University of Technology or Nicolaus Copernicus University

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Miscellaneous
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Conference
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Ceccaldi, D.
Meeting of the Societe de Chimie Physique. Radiation chemistry. Orsay, 27-28 October 1977
Meeting of the Societe de Chimie Physique. Radiation chemistry. Orsay, 27-28 October 1977
AbstractAbstract
No abstract available
Original Title
Luminescence differee d'une solution organique vitreuse photoactivee: une sonde des proprietes dynamiques de l'etat vitreux
Source
p. 34; nd; p. 34; Universite de Paris-11. Lab. Physico-Chimie des Rayonnements; Orsay, France; Meeting of the Societe de Chimie Physique. Radiation chemistry; Orsay, France; 27 - 28 Oct 1977; Published in abstract form only.
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Book
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AbstractAbstract
[en] Electron absorption and emission spectra have been obtained for ten aromatic derivatives of lithium, boron, aluminium and gallium in inert and electron-donor solvents at 295 and 77 deg K. The observed intensive long-wave bands, whose psrameters depend on a particular element, aromatic radical structure and solvent donor capacity, are associated with the electronic transitions in the aromatic system disturbed by an intra- and intermolecular charge transfer with participation of free p-orbitals of the element. A decrease in the total luminescent capacity of the examined molecules with the growth of atomic number of the element has been revealed, which can be accounted for by the heavy atom effect and a higher probability of various non-radiative processes, including molecular photodissociation along the C-M link
Original Title
Ehlektronnye spektry i struktura aromaticheskikh proizvodnykh litiya, bora, alyuminiya i galliya
Primary Subject
Source
For English translation see the journal Bull. Acad. Sci. USSR, Div. Chem. Sci.
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Journal Article
Journal
Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (no.9); p. 1993-1998
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Long, Wang; Xing, Chengzong; Xu, Li; Liu, Guoji, E-mail: wanglong3767@163.com, E-mail: xuli@zzu.edu.cn, E-mail: guojiliu@zzu.edu.cn2019
AbstractAbstract
[en] The article is published in the original.
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Copyright (c) 2019 Pleiades Publishing, Ltd.; Country of input: International Atomic Energy Agency (IAEA)
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Journal Article
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AbstractAbstract
[en] The use of ionic liquids as reaction media can confer many advantages upon catalytic reactions over reactions in organic solvents. In ionic liquids, catalysts having polar or ionic character can easily be immobilized without additional structural modification and thus the ionic solutions containing the catalyst can easily be separated from the reagents and reaction products, and then, be reused. More interestingly, switching from an organic solvent to an ionic liquid often results in a significant improvement in catalytic performance (e.g., rate acceleration, (enantio)selectivity improvement and an increase in catalyst stability). In this review, some recent interesting results which can nicely demonstrate these positive 'ionic liquid effect' on catalysis are discussed
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71 refs, 27 figs, 1 tab
Record Type
Journal Article
Journal
Bulletin of the Korean Chemical Society; ISSN 0253-2964;
; v. 26(9); p. 1321-1330

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AbstractAbstract
[en] Inductively coupled plasma atomic emission spectroscopy, is one of the most rapidly developing analytical techniques. Potential users show enormous interest in the three ICP models. Analytical results coming from various users, who adopted the technique, realised the potential of ICP. This resulted in a range of equipment available today which shows total dedication to the ICP technique
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Source
Addison, C. (ed.); 24 p; Feb 1982; p. 17; New Chemical Publications; Johannesburg
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Book
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Esch, R.A.
Fluor Daniel Hanford, Inc., Richland, WA (United States). Funding organisation: USDOE Office of Environmental Restoration and Waste Management, Washington, DC (United States)1997
Fluor Daniel Hanford, Inc., Richland, WA (United States). Funding organisation: USDOE Office of Environmental Restoration and Waste Management, Washington, DC (United States)1997
AbstractAbstract
[en] This document is the final laboratory report for tank 241-S-106 push mode core segments collected between February 12, 1997 and March 21, 1997. The segments were subsampled and analyzed in accordance with the Tank Push Mode Core Sampling and Analysis Plan (TSAP), the Tank Safety Screening Data Quality Objective (Safety DQO), the Historical Model Evaluation Data Requirements (Historical DQO) and the Data Quality Objective to Support Resolution of the Organic Complexant Safety Issue (Organic DQO). The analytical results are included in Table 1. Six of the twenty-four subsamples submitted for the differential scanning calorimetry (DSC) analysis exceeded the notification limit of 480 Joules/g stated in the DQO. Appropriate notifications were made. Total Organic Carbon (TOC) analyses were performed on all samples that produced exotherms during the DSC analysis. All results were less than the notification limit of three weight percent TOC. No cyanide analysis was performed, per agreement with the Tank Safety Program. None of the samples submitted for Total Alpha Activity exceeded notification limits as stated in the TSAP. Statistical evaluation of results by calculating the 95% upper confidence limit is not performed by the 222-S Laboratory and is not considered in this report. No core composites were created because there was insufficient solid material from any of the three core sampling events to generate a composite that would be representative of the tank contents
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Secondary Subject
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25 Jun 1997; 600 p; CONTRACT AC06-96RL13200; ALSO AVAILABLE FROM OSTI AS DE99050052; NTIS; US GOVT. PRINTING OFFICE DEP
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Report
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SANDGREN, K.R.
CH2M (US). Funding organisation: USDOE Office of Environmental Management (EM) (United States)2003
CH2M (US). Funding organisation: USDOE Office of Environmental Management (EM) (United States)2003
AbstractAbstract
[en] This technical basis document was developed to support the Tank Farms Documented Safety Analysis (DSA), and describes the risk binning process and the technical basis for assigning risk bins for the organic solvent fire representative and associated represented hazardous conditions. The purpose of the risk binning process is to determine the need for safety-significant structures, systems, and components (SSC) and technical safety requirement (TSR)-level controls for a given representative accident or represented hazardous conditions based on an evaluation of the frequency and consequence. Note that the risk binning process is not applied to facility workers, because all facility worker hazardous conditions are considered for safety-significant SSCs and/or TSR-level controls. Determination of the need for safety-class SSCs was performed in accordance with DOE-STD-3009-94, Preparation Guide for US Department of Energy Nonreactor Nuclear Facility Documented Safety Analyses, as described in this report
Primary Subject
Source
22 Mar 2003; 98 p; EDT--636630; AC--27-99RL14047; Available from PURL: https://www.osti.gov/servlets/purl/810662-dSRTdj/native/
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Report
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AbstractAbstract
[en] Polyynes were formed by laser ablation of a graphite target in deionized water (H2O and D2O) and various organic solvents such as acetonitrile, n-hexane, and c-hexane and were identified by analyzing ultraviolet (UV) absorption and Raman spectra. We assigned the major UV absorption peaks that coincided with the electronic transitions corresponding to linear polyyne chains. The UV absorption peak intensities of a polyyne solution decreased as the holding temperature of the solution increased. Also, the absorption spectra of polyynes obtained by laser ablation of a graphite target at different volume fractions of H2O and D2O were examined
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21 refs, 5 figs, 1 tab
Record Type
Journal Article
Journal
Bulletin of the Korean Chemical Society; ISSN 0253-2964;
; v. 33(2); p. 597-600

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Navratil, J.D.
Rockwell International Corp., Golden, CO (USA). Rocky Flats Plant1986
Rockwell International Corp., Golden, CO (USA). Rocky Flats Plant1986
AbstractAbstract
[en] Some aspects of solvent extraction chemistry in the field of nuclear technology are briefly reviewed. Applications of solvent extraction in actinide recovery and purification, radionuclide production, and reactor materials preparation are summarized. The need for new, more selective, solvent extraction reagents is presented via examples of recent work with bifunctional organophosphorus reagents applied to the removal of actinides from acidic radioactive waste solutions
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Secondary Subject
Source
1986; 9 p; Available from NTIS, PC A02/MF A01 as DE86009329
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Report
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