Relevant bibliographies by topics / Electron nuclear double resonance spectroscopy

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Electron nuclear double resonance spectroscopy'

Author: Grafiati
Published: 4 June 2021
Last updated: 28 January 2023

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Journal articles on the topic "Electron nuclear double resonance spectroscopy"

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Eachus, R. S., and M. T. Olm. "Electron Nuclear Double Resonance Spectroscopy." Science 230, no. 4723 (October 18, 1985): 268–74. http://dx.doi.org/10.1126/science.230.4723.268.

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Jeschke, Gunnar, and Arthur Schweiger. "Hyperfine-correlated electron nuclear double resonance spectroscopy." Chemical Physics Letters 246, no. 4-5 (December 1995): 431–38. http://dx.doi.org/10.1016/0009-2614(95)01202-4.

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Rizzato, Roberto, and Marina Bennati. "Cross-Polarization Electron-Nuclear Double Resonance Spectroscopy." ChemPhysChem 16, no. 18 (November 13, 2015): 3769–73. http://dx.doi.org/10.1002/cphc.201500938.

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Mchaourab, Hassane S., T. C. Christidis, and James S. Hyde. "Continuous wave multiquantum electron paramagnetic resonance spectroscopy. IV. Multiquantum electron–nuclear double resonance." Journal of Chemical Physics 99, no. 7 (October 1993): 4975–85. http://dx.doi.org/10.1063/1.465999.

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Fahnenschmidt, M., R. Bittl, H. K. Rau, W. Haehnel, and W. Lubitz. "Electron paramagnetic resonance and electron nuclear double resonance spectroscopy of a heme protein maquette." Chemical Physics Letters 323, no. 3-4 (June 2000): 329–39. http://dx.doi.org/10.1016/s0009-2614(00)00530-3.

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KURODA, SHIN-ICHI. "ELECTRON NUCLEAR DOUBLE RESONANCE SPECTROSCOPY OF SOLITONS AND POLARONS IN CONJUGATED POLYMERS." International Journal of Modern Physics B 09, no. 03 (January 30, 1995): 221–60. http://dx.doi.org/10.1142/s0217979295000124.

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Novel elementary excitations such as solitons and polarons in conjugated polymers carry unpaired electrons. In this case electron nuclear double resonance (ENDOR) of protons on the conjugated chain provides a unique method to observe their wavefunctions. This information has two significant meanings. Firstly, it gives the spatial extension of solitons and polarons, the quantity that is essential in examining the reality of these self-localized excitations. Secondly, it directly probes the degree of electron correlation. In the case of finite electron correlation, negative spin sites appear in the spin-density distribution. The unique and detailed determination of the wavefunctions containing such information can be made only after the careful studies of oriented polymers because of the non-single-crystalline nature of these materials. In this article I review our ENDOR studies on solitons in polyacetylene and polarons in poly(paraphenylene vinylene), performed using stretch-oriented samples. All the analyses are based on the properties of π-electrons which show characteristic anisotropy in oriented samples. The observed spin distributions are compared with theoretical results as well as shown as the basis for further analyses of conjugated polymers.
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Milić, Božidar Lj, Sonja M. Djilas, Pavle I. Premović, and Jasna M. Čanadanović-Brunet. "Electron spin resonance and electron nuclear double resonance spectroscopy study of non-dialysable melanoidin pyrolysates." Journal of Analytical and Applied Pyrolysis 21, no. 1-2 (September 1991): 233–37. http://dx.doi.org/10.1016/0165-2370(91)80028-7.

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Hoffman, B. M. "Electron-nuclear double resonance spectroscopy (and electron spin-echo envelope modulation spectroscopy) in bioinorganic chemistry." Proceedings of the National Academy of Sciences 100, no. 7 (March 17, 2003): 3575–78. http://dx.doi.org/10.1073/pnas.0636464100.

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Webb, Michael I., and Charles J. Walsby. "Albumin binding and ligand-exchange processes of the Ru(iii) anticancer agent NAMI-A and its bis-DMSO analogue determined by ENDOR spectroscopy." Dalton Transactions 44, no. 40 (2015): 17482–93. http://dx.doi.org/10.1039/c5dt02021b.

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Baker, G. J., P. F. Knowles, K. B. Pandeya, and J. B. Rayner. "Electron nuclear double-resonance (ENDOR) spectroscopy of amine oxidase from pig plasma." Biochemical Journal 237, no. 2 (July 15, 1986): 609–12. http://dx.doi.org/10.1042/bj2370609.

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Electron nuclear double-resonance (‘ENDOR’) spectroscopic studies on pig plasma amine oxidase have been carried out at 15 K. Deuterium-exchange studies show the presence of two sets of exchangeable protons, probably from two water molecules; from the magnitude of their hyperfine couplings, one is assigned to be equatorially, and the other axially, co-ordinated. Only one 14N hyperfine coupling is observed, suggesting that the bonding of all amino acid (histidine) or organic cofactor ligands is similar. Upon addition of azide, a further hyperfine coupling to nitrogen is observed which is smaller than that observed for the native enzyme; the hyperfine couplings to the remaining nitrogens are slightly altered.
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Dissertations / Theses on the topic "Electron nuclear double resonance spectroscopy"

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Reese, Annabelle Wey. "Analysis of CW-EPR spectra and the internal dynamics of DNA /." Thesis, Connect to this title online; UW restricted, 1996. http://hdl.handle.net/1773/8569.

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Young, Matthew Alexander. "A site-directed spin labelling study of the human alpha-lactalbumin molten globule." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:cdc9904d-77cc-4d20-b01d-096bc2b16d72.

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The human α-lactalbumin (α-LA) molten globule formed at low pH is a model for the study of protein folding intermediates. The molten globule lacks native-like side-chain interactions, resulting in a fluctuating ensemble of tertiary structures, characterisation of which has been precluded by severe line-broadening in NMR spectra and a lack of long-range NOEs. Paramagnetic relaxation enhancements (PREs) have been measured in a variant of α-LA in which all native cysteines have been mutated to alanine (all-Ala α-LA). Cysteine residues have been mutated into regions of interest and spin labelled with MTSL. These measurements have confirmed that all-Ala α-LA forms a compact molten globule. Transient, long-range interactions that are stabilising the compact fold have also been identified using PREs measured in urea-denatured states. This has identified several interactions formed by hydrophobic residues from both the α- and β-domain, which could be important for initiating and driving folding. The molten globule’s 3D topology has been probed by measuring long-range distances between MTSL pairs using Double Electron-Electron Resonance (DEER). Broad distance distributions have been identified between elements of secondary structure, indicative of a fluctuating but compact fold. By contrast, a narrower distance distribution has been measured within one of the major helices, indicative of native-like secondary structure. The surface accessibility of all-Ala α-LA and that of two other variants ([28-111] α-LA and 4SS α-LA) has been probed using solvent PREs obtained using TEMPOL, a paramagnetic co-solute. This has revealed differences in the solvent-exposure of hydrophobic residues due to the removal of disulphide bonds. This method has also identified buried hydrophobic residues that contribute to forming the molten globule’s stable, native-like core.
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Dorin, Catalina I. "Electron paramagnetic resonance and electron nuclear double resonance study of Nb⁵⁺ hole center in CdWO₄." Morgantown, W. Va. : [West Virginia University Libraries], 1999. http://etd.wvu.edu/templates/showETD.cfm?recnum=745.

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Thesis (M.S.)--West Virginia University, 1999.
Title from document title page. Document formatted into pages; contains ix, 72 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 40).
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Skrzypczak-Bonduelle, Audrey. "Les premières traces de vie sur Terre : une approche spectroscopique et mimétique du problème." Phd thesis, Paris 6, 2005. http://pastel.archives-ouvertes.fr/pastel-00001717.

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Stevens, Kevin T. "Electron-nuclear double resonance studies of point defects in AgGaSe₂ and ZnGeP₂." Morgantown, W. Va. : [West Virginia University Libraries], 1999. http://etd.wvu.edu/templates/showETD.cfm?recnum=1130.

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Thesis (Ph. D.)--West Virginia University, 1999.
Title from document title page. Document formatted into pages; contains ix, 165 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 118-122).
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Ramamurthy, Senthil. "Localized double-quantum filtered correlated spectroscopy on 3T MRI/MRS scanner." Morgantown, W. Va. : [West Virginia University Libraries], 2005. https://etd.wvu.edu/etd/controller.jsp?moduleName=documentdata&jsp%5FetdId=4012.

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Thesis (M.S.)--West Virginia University, 2005.
Title from document title page. Document formatted into pages; contains ix, 69 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 65-69).
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Wang, Hao. "Mechanistic studies of electrochemical double layer capacitors using solid-state NMR spectroscopy." Thesis, University of Cambridge, 2014. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.708302.

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Forino, Paola Caterina. "Nuclear magnetic resonance study of the electron doped Dirac-Mott Insulator double perovskite Ba2Na(1-x)CaxOsO6." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2020.

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Osmium-based materials exhibit unconventional magnetism due to the interplay between spin orbit coupling and strong electronic correlations. In this thesis we investigate for the first time the effect of charge doping on the Dirac Mott insulator double perovskites Ba2Na(1-x)CaxOsO6 by using Nuclear Magnetic Resonance technique. We study in details the evolution of the magnetic phase diagram as a function of doping and applied magnetic field. The system rapidly evolves from a canted to a collinear antiferromagnetic ground state with a monotonic increase of the magnetic transition temperature. Furthermore, the system remains insulating in the whole range of doping, despite the injection of extra electrons. This indicates that the Dirac-Mott insulating state of this material is unusually robust. In particular, the results show an unexpected thermally activated charge dynamics which suggests the presence of polarons dominating the high temperature excitations of this Dirac-Mott insulator.
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Drew, Daniel L. Jr. "Investigating the Structure and Dynamic Properties of Bacteriophage S21 Pinholin Using Solid-State Nuclear Magnetic Resonance and Electron Paramagnetic Resonance Spectroscopy." Miami University / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=miami1610187893016095.

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Worthoff, Wieland Alexander [Verfasser]. "Dynamics of Electron and Nuclear Spin Interaction in Laser Assisted Nuclear Magnetic Resonance Spectroscopy of Gallium Arsenide Nanostructures / Wieland Alexander Worthoff." Aachen : Shaker, 2011. http://d-nb.info/1070150576/34.

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Books on the topic "Electron nuclear double resonance spectroscopy"

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Shi yong dian zi ci gong zhen bo pu xue: Ji ben yuan li he shi ji ying yong. Beijing: Ke xue chu ban she, 2008.

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Lowe, David John. ENDOR and EPR of metalloproteins. New York: Springer-Verlag, 1995.

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P, Poole Charles, and Farach Horacio A, eds. Handbook of electron spin resonance: Data sources, computer technology, relaxation, and ENDOR. New York: American Institute of Physics, 1994.

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1951-, Kirste Burkhard, and Lubitz Wolfgang 1949-, eds. Electron nuclear double resonance spectroscopy of radicals in solution: Application to organic and biological chemistry. New York: VCH, 1988.

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D, Yordanov N., ed. Proceedings of the International Workshop on Electron Magnetic Resonance of Disordered Systems (EMARDIS-89) Pravet͡z, Bulgaria, July 7-10, 1989. Singapore: World Scientific, 1989.

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6

Gurbiel, Ryszard J. Badania struktury wybranych metaloenzymów przy użyciu metody podwójnego rezonansu elektronowo-jądrowego (ENDOR). Kraków: Wydawn. Uniwersytetu Jagiellońskiego, 1997.

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Poole, Charles P. Electron spin resonance: A comprehensive treatise on experimental techniques. Mineola, N.Y: Dover Publications, 1996.

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Spaeth, Johann-Martin. Structural analysis of point defects in solids: An introduction to multiple magnetic resonance spectroscopy. Berlin: Springer-Verlag, 1992.

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Brossel, Jean. Optical methods in atomic physics: Historical perspectives and a few new trends. Mainz: Akademie der Wissenschaften und der Literatur, 1992.

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Transition ion electron paramagnetic resonance. Oxford: Clarendon Press, 1990.

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Book chapters on the topic "Electron nuclear double resonance spectroscopy"

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Thomson, A. J. "Electron Paramagnetic Resonance and Electron Nuclear Double Resonance Spectroscopy." In Perspectives in Modern Chemical Spectroscopy, 295–320. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-75456-2_12.

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Thomann, Hans, and Marcelino Bernardo. "Advances in Electron Nuclear Double Resonance Spectroscopy." In Advances in Chemistry, 65–90. Washington, DC: American Chemical Society, 1992. http://dx.doi.org/10.1021/ba-1993-0229.ch004.

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Kuroda, S., K. Murata, Y. Shimoi, S. Abe, T. Noguchi, and T. Ohnishi. "Electron-Nuclear Double-Resonance Spectroscopy of Polarons in Conjugated Polymers." In Springer Proceedings in Physics, 256–67. Tokyo: Springer Japan, 1996. http://dx.doi.org/10.1007/978-4-431-68470-1_20.

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Thomann, Hans, Marcelino Bernardo, and Bernard G. Silbernagel. "Pulsed Electron Nuclear Double Resonance Spectroscopy of Argonne Premium Coals." In Advances in Chemistry, 561–80. Washington, DC: American Chemical Society, 1992. http://dx.doi.org/10.1021/ba-1993-0229.ch030.

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Chen, Xinhua, Hugh McManus, and Larry Kevan. "Electron Spin Resonance, Electron Nuclear Double Resonance, and Electron Spin-Echo Spectroscopic Studies of Argonne Premium Coals." In Advances in Chemistry, 451–66. Washington, DC: American Chemical Society, 1992. http://dx.doi.org/10.1021/ba-1993-0229.ch024.

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Thomann, Hans, and Marcelino Bernardo. "Pulsed Electron Nuclear Double and Multiple Resonance Spectroscopy of Metals in Proteins and Enzymes." In EMR of Paramagnetic Molecules, 275–322. Boston, MA: Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2892-0_7.

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Spaeth, Johann-Martin, and Harald Overhof. "Electron Nuclear Double Resonance." In Point Defects in Semiconductors and Insulators, 163–95. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-642-55615-9_5.

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Spaeth, Johann-Martin, Jürgen R. Niklas, and Ralph H. Bartram. "Electron Nuclear Double Resonance." In Springer Series in Solid-State Sciences, 139–68. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-84405-8_5.

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McWhinnie, William R. "Electron Spin Resonance and Nuclear Magnetic Resonance Applied to Minerals." In Chemical Bonding and Spectroscopy in Mineral Chemistry, 209–49. Dordrecht: Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-009-4838-9_6.

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Bode, B. E., and D. G. Norman. "Pulsed Electron-Electron Double Resonance (PELDOR) and Electron Spin Echo Envelope Modulation (ESEEM) Spectroscopy in Bioanalysis." In Radiation in Bioanalysis, 195–212. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-28247-9_7.

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Conference papers on the topic "Electron nuclear double resonance spectroscopy"

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Marleau, Peter, James Brennan, Erik Brubaker, Wondwosen Mengesha, and Stanley Mrowka. "Fast neutron resonance tomography using double scatter spectroscopy for materials identification." In 2011 IEEE Nuclear Science Symposium and Medical Imaging Conference (2011 NSS/MIC). IEEE, 2011. http://dx.doi.org/10.1109/nssmic.2011.6154501.

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Sato, Kazuo, Shigeki Nakazawa, Robabeh D. Rahimi, Shinsuke Nishida, Tomoaki Ise, Daisuke Shimoi, Kazuo Toyota, et al. "QUANTUM COMPUTING USING PULSE-BASED ELECTRON-NUCLEAR DOUBLE RESONANCE (ENDOR): MOLECULAR SPIN-QUBITS." In Molecular Realizations of Quantum Computing 2007. WORLD SCIENTIFIC, 2009. http://dx.doi.org/10.1142/9789812838681_0004.

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FURUKAWA, T., T. SHIMODA, Y. MATSUO, Y. FUKUYAMA, T. KOBAYASHI, A. HATAKEYAMA, T. ITOU, and Y. OTA. "LASER-MICROWAVE DOUBLE RESONANCE SPECTROSCOPY IN SUPERFLUID HELIUM FOR THE MEASUREMENT OF NUCLEAR MOMENTS." In Proceedings of the Eleventh International Workshop. WORLD SCIENTIFIC, 2007. http://dx.doi.org/10.1142/9789812770653_0031.

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Fernandez-Gutierrez, S., Dennis Gautreau, and J. R. Sirigiri. "263 GHz Traveling Wave Tube (TWT) amplifier for Dynamic Nuclear Polarization (DNP) and Electron Paramagnetic Resonance (EPR) spectroscopy." In 2015 40th International Conference on Infrared, Millimeter, and Terahertz waves (IRMMW-THz). IEEE, 2015. http://dx.doi.org/10.1109/irmmw-thz.2015.7327797.

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Chen, Wen An, Dai Guo Yu, Guo Liang Liu, Qing Bo Li, Di Zhang, Meng Zhao, Fang fang Wu, et al. "Evaluating Complex Lacustrine Carbonate Reservoir by Integrating Advanced Logging Techniques and Core Measurements-A Case Study in Qiadam Basin." In SPE Reservoir Characterisation and Simulation Conference and Exhibition. SPE, 2023. http://dx.doi.org/10.2118/212607-ms.

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Abstract A complex and tight lacustrine carbonate reservoir is the main target reservoir in Qaidam Basin. The diagenesis of shallow-shore lake deposition has created a highly heterogeneous reservoir in both vertical and horizontal directions in terms of lithologies, pore structures, and permeability. The core analysis shows a wide variety of lithologies that include terrigenous clastics (quartz, orthoclase, and plagioclase), carbonate (calcite, dolomite, and ankerite), and evaporite minerals such as anhydrite, etc. Electron microscope analysis shows mainly intercrystallite pores with dolomite, dissolved pores, and microfractures. Associated with the complex lithology and pore structure, reservoir permeability is varied and is mostly less than 0.02mD. Evaluating and characterizing this complex reservoir to find a better pay zone was the objective of this study. To evaluate the lithologies, pore structures, porosities, and permeability in quantities accurately, the advanced gamma-ray spectroscopy logs, nuclear magnetic resonance (NMR) logs, and high-resolution micro-resistivity borehole image logs were acquired in some key wells. Integrated with core data such as X-ray diffraction (XRD), mercury injection capillary (MICP), the lithofacies, texture facies, and pore facies were classified based on the minerals from gamma-ray spectroscopy, the textures from borehole image, and the pore sizes from NMR. The combination of these three facies represents the reservoir quality. In the study area, the lithofacies were classified into four types, which are high carbonate content facies, middle carbonate content facies, high clay content facies, and high clastic content facies. The texture facies were classified into four types, which are massive texture, layered texture, dissolved texture, and algal texture. The pore structure facies were classified into four types, which are macro facies, meso facies, meso-micro facies, and microfacies. The better pay zone is the combination of high carbonate content facies, algal texture, and macro facies. The pay zone of the reservoir was well defined and mapped with the combination facies vertically and horizontally in the whole study area. The integrated solution described in this study leverages the advantages of advanced gamma-ray spectroscopy, NMR, borehole images, and core measurements. It develops a comprehensive understanding of the complex carbonate reservoir and provides the solution to pinpoint the sweet spots and place the horizontal well.
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Lumetta, Gregg J., Brian M. Rapko, and Herman M. Cho. "Studies of the Fundamental Chemistry of Hanford Tank Sludges." In ASME 2003 9th International Conference on Radioactive Waste Management and Environmental Remediation. ASMEDC, 2003. http://dx.doi.org/10.1115/icem2003-4633.

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The U.S. Department of Energy has embarked on an effort to retrieve, immobilize, and dispose of the 2.1 × 105 m3 of radioactive tank wastes that were generated during weapons production and other operations at the Hanford Site in Washington State. One of the major challenges associated with this effort is the processing of the 4.2 × 104 m3 of high-level waste sludges. These sludges consist of a complex mixture of amorphous and crystalline mineral phases. The current plan for processing the sludge solids consists of leaching with aqueous NaOH, washing out the NaOH and dissolved components, then vitrifying the solids in borosilicate glass. The purpose of the NaOH leaching step is to remove components such as Al, Cr, and P that can lead to the production of an unacceptable quantity of high-level waste glass. In this paper, we will discuss the chemistry underlying the leaching and washing processes, focusing on the specific mineral phases present in the sludge solids and how these phases respond to the leaching process. The chemical phases present in the Hanford tank sludge solids have been identified through microscopy coupled with electron diffraction and through powder X-ray diffraction. We have also recently been applying nuclear magnetic resonance spectroscopy to characterize chemical species in tank sludge solids. Numerous chemical species have been identified including the aluminum oxy/hydroxides gibbsite and boehmite, aluminosilicates, iron oxy/hydroxides, and mixed Cr/Fe oxyhydroxides. Identification of these phases has led to a more fundamental understanding of the behavior of the various sludge components during leaching; in turn, this understanding will allow for improved process flow sheets. For example, we have shown that certain tank sludges are high in boehmite, Υ-AIOOH. This mineral phase is much more refractory than other AI phases such as gibbsite. Thus, more severe leaching conditions (e.g., increased temperature, NaOH concentration, and leaching duration) are required to remove AI from wastes high in boehmite.
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Chai, Rukaun, Yuetian Liu, Qianjun Liu, Xuan He, and Pingtian Fan. "Effect and Mechanism of CO2 Electrochemical Reduction for CCUS-EOR." In SPE Annual Technical Conference and Exhibition. SPE, 2021. http://dx.doi.org/10.2118/206135-ms.

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Abstract Unconventional reservoir plays an increasingly important role in the world energy system, but its recovery is always quite low. Therefore, the economic and effective enhanced oil recovery (EOR) technology is urgently required. Moreover, with the aggravation of greenhouse effect, carbon neutrality has become the human consensus. How to sequestrate CO2 more economically and effectively has aroused wide concerns. Carbon Capture, Utilization and Storage (CCUS)-EOR is a win-win technology, which can not only enhance oil recovery but also increase CO2 sequestration efficiency. However, current CCUS-EOR technologies usually face serious gas channeling which finally result in the poor performance on both EOR and CCUS. This study introduced CO2 electrochemical conversion into CCUS-EOR, which successively combines CO2 electrochemical reduction and crude oil electrocatalytic cracking both achieves EOR and CCUS. In this study, multiscale experiments were conducted to study the effect and mechanism of CO2 electrochemical reduction for CCUS-EOR. Firstly, the catalyst and catalytic electrode were synthetized and then were characterized by using scanning electron microscope (SEM) & energy dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS). Then, electrolysis experiment & liquid-state nuclear magnetic resonance (1H NMR) experiments were implemented to study the mechanism of CO2 electrochemical reduction. And electrolysis experiment & gas chromatography (GC) & viscosity & density experiments were used to investigate the mechanism of crude oil electrocatalytic cracking. Finally, contact angle and coreflooding experiments were respectively conducted to study the effect of the proposed technology on wettability and CCUS-EOR. SEM & EDS & XPS results confirmed that the high pure SnO2 nanoparticles with the hierarchical, porous structure, and the large surface area were synthetized. Electrolysis & 1H NMR experiment showed that CO2 has converted into formate with the catalysis of SnO2 nanoparticles. Electrolysis & GC & Density & Viscosity experiments indicated that the crude oil was electrocatalytically cracked into the light components (<C20) from the heavy components (C21∼C37). As voltage increases from 2.0V to 7.0V, the intensity of CO2 electrocchemical reduction and crude oil electrocatalytic cracking enhances to maximum at 3.5V (i.e., formate concentration reaches 6.45mmol/L and carbon peak decreases from C17 to C15) and then weakens. Contact angle results indicated that CO2 electrochemical reduction and crude oil electocatalytic cracking work jointly to promote wettability alteration. Thereof, CO2 electrochemical reduction effect is dominant. Coreflooding results indicated that CO2 electrochemical reduction technology has great potential on EOR and CCUS. With the SnO2 catalytic electrode at optimal voltage (3.5V), the additional recovery reaches 9.2% and CO2 sequestration efficiency is as high as 72.07%. This paper introduced CO2 electrochemical conversion into CCUS-EOR, which successfully combines CO2 electrochemical reduction and crude oil electrocatalytic cracking into one technology. It shows great potential on CCUS-EOR and more studies are required to reveal its in-depth mechanisms.
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Reports on the topic "Electron nuclear double resonance spectroscopy"

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Belford, R. L., and R. B. Clarkson. Spin-mapping of coal structures with ESE (Electron Spin Echo) and ENDOR (Electron-Nuclear Double Resonance). Office of Scientific and Technical Information (OSTI), December 1988. http://dx.doi.org/10.2172/6409289.

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Belford, R. L., and R. B. Clarkson. Spin-mapping of coal structures with ESE and ENDOR (electron nuclear double resonance). Office of Scientific and Technical Information (OSTI), June 1989. http://dx.doi.org/10.2172/6355326.

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Belford, R. L., and R. B. Clarkson. Spin-mapping of coal structures with ESE and ENDOR (Electron-Nuclear Double Resonance). Office of Scientific and Technical Information (OSTI), March 1989. http://dx.doi.org/10.2172/6501445.

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You might also be interested in the extended bibliographies on the topic 'Electron nuclear double resonance spectroscopy' for particular source types:
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