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Harris, J.M.
Sandia National Labs., Albuquerque, NM (United States). Funding organisation: USDOE, Washington, DC (United States)1995
Sandia National Labs., Albuquerque, NM (United States). Funding organisation: USDOE, Washington, DC (United States)1995
AbstractAbstract
[en] The following annotated bibliography lists documents prepared by the Department of Energy (DOE), and predecessor agencies, to meet the requirements of the National Environmental Policy Act (NEPA) for activities and facilities at Sandia National Laboratories sites. For each NEPA document summary information and a brief discussion of content is provided. This information may be used to reduce the amount of time or cost associated with NEPA compliance for future Sandia National Laboratories projects. This summary may be used to identify model documents, documents to use as sources of information, or documents from which to tier additional NEPA documents
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Apr 1995; 25 p; CONTRACT AC04-94AL85000; Also available from OSTI as DE95011830; NTIS; US Govt. Printing Office Dep
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Bibliography
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Borders, J.A.; Harris, J.M.
Sandia Labs., Albuquerque, N.Mex. (USA)1977
Sandia Labs., Albuquerque, N.Mex. (USA)1977
AbstractAbstract
[en] The use of nuclear reactions for depth profiling carbon and oxygen in solids is discussed. A general expression for the yield from a nuclear reaction is derived and used to extract depth profiles from the energy spectra by two methods. The first method compares data from a target of unknown composition with a target containing a known concentration of either carbon or oxygen. By dividing the yields from the samples for equal collision energies, a concentration profile within the analyzed sample can be obtained. The second method uses published reaction cross section data to obtain the profile. The (d,p) profiling is demonstrated for carbon in ScD2. A comparison between the two methods is made by extracting carbon profiles in the near surface region of ScD2 samples. Effects due to inaccurate stopping cross section data are described. The technique is discussed for the 16O(d,p) reactions used to profile oxygen along with the effect of interferences from the 2H(d,p)3H reaction and other reactions
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Source
1977; 20 p; 3. international conference on ion beam analysis; Washington, District of Columbia, United States of America (USA); 27 Jun - 1 Jul 1977; CONF-770642--4; Available from NTIS., PC A02/MF A01
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AbstractAbstract
No abstract available
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Journal Article
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Applied Physics Letters; v. 21(12); p. 598-601
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Harris, J.M.; Miller, J.R.; Frazier, R.S.; Walter, J.H.
Rockwell International Corp., Canoga Park, CA (USA). Energy Systems Group1982
Rockwell International Corp., Canoga Park, CA (USA). Energy Systems Group1982
AbstractAbstract
[en] This paper presents the results and observations of a study performed by the authors to parametrically evaluate the performance characteristics of a foam process for application of decontamination agents. The initial tests were established to assess foam quality. Subsequent tests determined the ability of the foam as a carrier of chemical systems, and established system operating parameters. The technique was then applied in an actual decontamination task to verify effectiveness of these established parameters and to determine decontamination reduction factors. 4 figures, 5 tables
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Source
1982; 14 p; International conference on decontamination of nuclear facilities; Niagara Falls (Canada); 19-22 Sep 1982; Available from NTIS, PC A02/MF A01; 1 as DE83016076
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Report
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Conference; Numerical Data
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AbstractAbstract
[en] This study examines the influence of the properties of various vascular graft materials on the bacterial adherence process of two different strains of Staphylococcus epidermidis (mucous and normucous producing). Dacron grafts (both knitted and woven), Teflon grafts, and Dacron grafts coated with one and two layers of silicone were studied because these materials differ significantly in porosity, hydrophobicity, and surface charge (zeta potential). Graft segments were immersed in 3H-labeled bacteria solution for periods ranging from 5 to 180 minutes and liquid scintillation techniques were used to quantify bacterial adherence. The porous knitted Dacron material had a significantly higher rate of bacterial adherence than either the woven Dacron or Teflon (p less than 0.05). Silicone coating (either one or two layers) reduced adherence by a factor of four for the knitted Dacron (p less than 0.05) and by a factor of two for woven Dacron (p less than 0.05). The mucous producing strain of S. epidermidis displayed significantly better adherence to woven and knitted Dacron than the normucous producing strain, but only when 0.25% dextrose was added to the bacteria solution. These findings indicate that the highly porous knitted Dacron grafts have the highest propensity for bacterial adhesion. Graft materials with the most negative zeta potentials are more resistant to bacterial adherence. Silicone coating of Dacron material significantly changed adherence characteristics, suggesting that this may be a viable strategy for protecting implantable medical devices containing materials to which bacteria readily adhere
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Journal Article
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AbstractAbstract
[en] The use of nuclear reactions for depth profiling carbon and oxygen in solids is discussed. A general expression for the yield from a nuclear reaction is derived and used to extract depth profiles from the energy spectra by two methods. The first method compares data from a target of unknown composition with a target containing a known concentration of either carbon or oxygen. By dividing the yields from the samples for equal collision energies, a concentration profile within the analyzed sample can be obtained. The second method uses published reaction cross-section data to obtain the profile. The (d, p) profiling is demonstrated for carbon in ScD2. A comparison between the two methods is made by extracting carbon profiles in the near surface region of ScD2 samples. Effects due to inaccurate stopping cross-section data are described. The technique is discussed for the 16O(d, p) reactions used to profile oxygen along with the effect of interferences from the 2H(d, p)3H reaction and other reactions. (Auth.)
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Source
3. international conference on ion beam analysis; Washington, D.C., USA; 27 Jun - 1 Jul 1977
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Journal Article
Literature Type
Conference
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Nuclear Instruments and Methods; v. 149(1-3); p. 279-284
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BARYONS, CATIONS, CHARGED PARTICLES, CHEMICAL ANALYSIS, DIMENSIONS, ELEMENTARY PARTICLES, ELEMENTS, ENERGY RANGE, EVEN-ODD NUCLEI, FERMIONS, HADRONS, HYDROGEN IONS, HYDROGEN IONS 1 PLUS, IONS, ISOTOPES, LIGHT NUCLEI, MEASURING INSTRUMENTS, MEV RANGE, NONMETALS, NUCLEAR REACTIONS, NUCLEI, NUCLEONS, OXYGEN ISOTOPES, RADIATION DETECTORS, SEMICONDUCTOR DETECTORS, SPECTRA, STABLE ISOTOPES, TARGETS
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AbstractAbstract
[en] The Prompt Gamma Neutron Activation Analysis (PGAA) technique yields elemental composition data which can be used to calculate the macroscopic cross section for any sample. The Small Sample Reactivity Measurements (SSRM) technique yields the macroscopic thermal absorption directly. Experimentally, PGAA is somewhat more difficult because of the calibration and data handling than is SSRM. However, SSRM requires a mathematical model of the reactor which means a rather complicated analysis. Once the model and calibration are completed, data analysis is routine. The SSRM technique is production oriented. 9 figures
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Source
Jennings, J.B.; Carroll, H.B. Jr. (eds.); USDOE Bartlesville Energy Technology Center, OK; p. 82-97; Apr 1982; p. 82-97; Western tight gas sands advanced logging workshop; Tulsa, OK (USA); 17 - 18 Mar 1981; Available from NTIS., PC A12/MF A01 as DE82014589
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Conference
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BARYON REACTIONS, BARYONS, CHEMICAL ANALYSIS, ELECTROMAGNETIC RADIATION, ELEMENTARY PARTICLES, ENRICHED URANIUM REACTORS, FERMIONS, GAMMA RADIATION, HADRON REACTIONS, HADRONS, IONIZING RADIATIONS, NEUTRONS, NUCLEAR REACTIONS, NUCLEON REACTIONS, NUCLEONS, POOL TYPE REACTORS, RADIATIONS, REACTORS, RESEARCH AND TEST REACTORS, RESEARCH REACTORS, ROCKS, SEDIMENTARY ROCKS, THERMAL REACTORS, WATER COOLED REACTORS, WATER MODERATED REACTORS
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AbstractAbstract
No abstract available
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Journal Article
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Applied Physics Letters; v. 26(1); p. 16-18
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No abstract available
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Phys. Rev., B; v. 11(3); p. 1013-1019
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[en] The behavior of Ti--Mo--Au metallization on Al2O3 and C was investigated by backscattering spectrometry. Results show that Mo--Au bimetal films typically mix during deposition. Diffusion of Ti in Mo film occurs at 6000C, but is inhibited by the presence of oxygen in the Ti film. Even 1000 A of Mo is not a barrier against interdiffusion of Ti and Au during 20-min anneals at 6000C. The amount of mixing observed also depends on the nature of the substrate which supports the Ti--Mo--Au metallization. (U.S.)
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Journal of Vacuum Science and Technology; v. 12(1); p. 524-527
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