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Готові списки джерел за темами / Group 13

Добірка наукової літератури з теми "Group 13"

Автор: Grafiati

Опубліковано: 10 грудня 2022

Оновлено: 28 січня 2023

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Статті в журналах з теми "Group 13"

1

Schulz, Stephan, Andreas Kuczkowski, Daniella Schuchmann, Ulrich Flörke, and Martin Nieger. "Group 13−Group 13 Donor−Acceptor Complexes." Organometallics 25, no. 22 (October 2006): 5487–91. http://dx.doi.org/10.1021/om0606946.

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2

Atwood, David A. "Cationic group 13 complexes." Coordination Chemistry Reviews 176, no. 1 (September 1998): 407–30. http://dx.doi.org/10.1016/s0010-8545(98)00127-1.

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3

Macdonald, Charles L. B., John D. Gorden, Andreas Voigt, Silvia Filipponi, and Alan H. Cowley. "Group 13 decamethylmetallocenium cations." Dalton Trans., no. 9 (2008): 1161–76. http://dx.doi.org/10.1039/b716220k.

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4

Cowley, Alan H. "From group 13–group 13 donor–acceptor bonds to triple-decker cations." Chem. Commun., no. 21 (2004): 2369–75. http://dx.doi.org/10.1039/b409497m.

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5

Cultrara, Nicholas D., Maxx Q. Arguilla, Shishi Jiang, Chuanchuan Sun, Michael R. Scudder, R. Dominic Ross, and Joshua E. Goldberger. "Group-13 and group-15 doping of germanane." Beilstein Journal of Nanotechnology 8 (August 9, 2017): 1642–48. http://dx.doi.org/10.3762/bjnano.8.164.

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Germanane, a hydrogen-terminated graphane analogue of germanium has generated interest as a potential 2D electronic material. However, the incorporation and retention of extrinsic dopant atoms in the lattice, to tune the electronic properties, remains a significant challenge. Here, we show that the group-13 element Ga and the group-15 element As, can be successfully doped into a precursor CaGe2 phase, and remain intact in the lattice after the topotactic deintercalation, using HCl, to form GeH. After deintercalation, a maximum of 1.1% As and 2.3% Ga can be substituted into the germanium lattice. Electronic transport properties of single flakes show that incorporation of dopants leads to a reduction of resistance of more than three orders of magnitude in H2O-containing atmosphere after As doping. After doping with Ga, the reduction is more than six orders of magnitude, but with significant hysteretic behavior, indicative of water-activation of dopants on the surface. Only Ga-doped germanane remains activated under vacuum, and also exhibits minimal hysteretic behavior while the sheet resistance is reduced by more than four orders of magnitude. These Ga- and As-doped germanane materials start to oxidize after one to four days in ambient atmosphere. Overall, this work demonstrates that extrinsic doping with Ga is a viable pathway towards accessing stable electronic behavior in graphane analogues of germanium.

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6

Munoz-Hernandez, Miguel-Angel, Pingrong Wei, Shengming Liu, and David A. Atwood. "Tetrametallic Group 13 ‘Mitsubishi’ Molecules." Coordination Chemistry Reviews 210, no. 1 (December 2000): 1–10. http://dx.doi.org/10.1016/s0010-8545(00)00314-3.

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7

Roberson, Loriann, Benjamin M. Galvin, and Atira Cherise Charles. "13 When Group Identities Matter." Academy of Management Annals 1, no. 1 (December 2007): 617–50. http://dx.doi.org/10.5465/078559818.

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8

Roberson, Loriann, Benjamin M. Galvin, and Atira Cherise Charles. "13 When Group Identities Matter." Academy of Management Annals 1, no. 1 (December 2007): 617–50. http://dx.doi.org/10.1080/078559818.

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9

Chitsaz, Soheila, and Bernhard Neumüller. "BINOL Compounds of Group 13." Organometallics 20, no. 11 (May 2001): 2338–43. http://dx.doi.org/10.1021/om010042b.

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10

Thomas, Florian, Stephan Schulz, Heidi Mansikkamäki, and Martin Nieger. "Unexpected Rearrangement Reaction of Lewis Base Stabilized Group 13/15 Compounds with Group 13 Trialkyls." Organometallics 22, no. 17 (August 2003): 3471–77. http://dx.doi.org/10.1021/om0303451.

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Дисертації з теми "Group 13"

1

Bullock, Thomas Hornsby. "Group 13 tris-pyridyl complexes." Thesis, University of Cambridge, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578971.

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2

Silverman, Joel Samuel. "Adventures in group 13 chemistry /." Digital version accessible at:, 1999. http://wwwlib.umi.com/cr/utexas/main.

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3

Mitra, Amitabha. "GROUP 13 CHELATES IN PHOSPHATE DEALKYLATION." UKnowledge, 2006. http://uknowledge.uky.edu/gradschool_diss/293.

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A series of mononuclear boron halides of the type LBX2 (LH = N-phenyl-3,5-di-tbutylsalicylaldimine,X = Cl (2), Br (3)) and LBX ( LH2 = N-(2-hydroxyphenyl)-3,5-di-tbutylsalicylaldimine,X = Cl (7), Br (8); LH2 = N-(2-hydroxyethyl)-3,5-di-tbutylsalicylaldimine,X = Cl (9), Br (10); LH2= N-(3-hydroxypropyl)-3,5-di-tbutylsalicylaldimine,X = Cl (11), Br (12)) were synthesized from their borate precursorsLB(OMe)2 (1) (LH = N-phenyl-3,5-di-t-butylsalicylaldimine ) and LB(OMe) (LH2 = N-(2-hydroxyphenyl)-3,5-di-t-butylsalicylaldimine (4), N-(2-hydroxyethyl)-3,5-di-tbutylsalicylaldimine(5), N-(3-hydroxypropyl)-3,5-di-t-butylsalicylaldimine (6)). Theborate precursors, 1, 4 - 6, in turn, were prepared by refluxing the corresponding ligandsLH or LH2 with excess B(OMe)3. The boron halide compounds were air- and moisturesensitiveand compound 7 on hydrolysis gave the oxo-bridged compound 13 thatcontained two seven-membered boron heterocycles. The boron halide compoundsdealkylated trimethyl phosphate in stoichiometric reactions to produce methyl halide andunidentified phosphate materials. Compounds 8 and 12 were found to be the mosteffective dealkylating agents. Compound 8 on reaction with t-butyl diphenyl phosphinateproduced a unique boron phosphinate compound LB(O)OPPh2 (14) containing a terminalphosphinate group. Compounds 1-14 were characterized by 1H, 13C, 11B, 31P NMR, IR,MS, EA and MP. Compounds 5, 6, 11, 12 and 13 were also characterized by singlecrystalX-ray diffraction.The alkane elimination reaction between Salen(tBu)H2 ligands and diethylaluminumbromide was used to prepare the four Salen aluminum bromide compounds,salen(tBu)AlBr (15) (salen = N,N'-ethylenebis(3,5-di-tert-butylsalicylideneimine)),salpen(tBu)AlBr (16) (salpen = N,N'-propylenebis(3,5-di-tert-butylsalicylideneimine)),salben(tBu)AlBr (17) (salben = N,N'-butylenebis(3,5-di-tert-butylsalicylideneimine)) andsalophen(tBu)AlBr (18) (salophen = N,N'-o-phenylenenebis(3,5-di-tertbutylsalicylideneimine)).The compounds contained five-coordinate aluminum either in adistorted square planar or a trigonal bipyramidal environment. The bromide group inthese compounds could be displaced by triphenylphosphine oxide or triphenyl phosphateto produce the six-coordinate cationic aluminum compounds [salen(tBu)Al(Ph3PO)2]Br(19), [salpen(tBu)Al(Ph3PO)2]Br (20), [salophen(tBu)Al(Ph3PO)2]Br (21) and[salophen(tBu)Al{(PhO)3PO}2]Br (22). All the compounds were characterized by 1H,13C, 27Al and 31P NMR, IR, mass spectrometry and melting point. Furthermore,compounds 15, 16, 17, 18, 20, 21 and 22 were structurally characterized by single-crystalX-ray diffraction. Compounds 15, 17 and 18 dealkylated a series of organophosphates instoichiometric reaction by breaking the ester C–O bond. Also, they promoted thedealkylation reaction between trimethyl phosphate and added boron tribromide.Stoichiometric reaction of compound 15 with trimethyl phosphate produced thealuminophosphinate compound salen(tBu)AlOP(O)Ph2 (23). Compound 16 on reactionwith tributyl phosphate produced the aluminophosphate compound[salpen(tBu)AlO]2[(BuO)2PO]2 (24). Compounds 23 and 24 were characterized by singlecrystalX-ray diffraction and spectroscopically.

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4

Tombul, Mustafa. "Towards heterometallic group 13 imido complexes." Thesis, University of Cambridge, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.620961.

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5

Ahmed, Shabana Almas. "Bis(phosphinimino) derivatives for Group 2 and Group 13 metals." Thesis, Imperial College London, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.434915.

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6

Bakewell, Clare Michelle. "Group 3 and Group 13 initiators for rac-lactide ring-opening polymerization." Thesis, Imperial College London, 2013. http://hdl.handle.net/10044/1/27290.

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This thesis describes the synthesis of a series of bis(quinolinolato)aluminium ethyl, (quinolinolato) gallium and (quinolinolato)zinc ethyl compounds which have been synthesised and fully characterised using spectroscopic techniques, elemental analyses and in some cases single crystal X-ray diffraction. The compounds are shown to be active initiators for the ring-opening polymerization of rac-lactide, with the activity being dependent on the metal, zinc > gallium > aluminium. All initiators show characteristics consistent with a controlled polymerization: predictable molecular weights and narrow polydispersities. The bis(quinolinolato)aluminium ethyl initiators all promote iso-selective ring-opening, with iso-selectivity values between 0.57 and 0.76. The degree of iso-selectivity is attributed to the steric hindrance imposed by the substituents on the ligands. The related gallium compounds show increased activity, whilst maintaining the good degree of stereocontrol. A series of yttrium phosphasalen compounds are also described and their activity for the ring-opening polymerization of rac-lactide is reported. The series of compounds vary at the diimine linker, the phenoxide substituents and at the alkoxide group. The compounds all show the rapid and controlled initiation of the ring-opening polymerization of lactide. The activity of the initiators was found to be dependent on the diimine linker: ethylene > cyclohexene > phenylene > propylene, and on the electron donating ability of the phenoxide substituent. All the initiators exerted a good degree of stereocontrol on the polymerization. Interestingly, the tacticity of the polymer was seen to switch from heterotactic polylactide (Ps 0.87) to isotactic polylactide (Pi 0.86), with the inclusion of an additional bonding nitrogen moiety in the diimine linker. The formation of isotactic polylactide using Group 3 initiators is extremely rare.

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7

Ong, Christopher M. "Group 13 and 14 imine and phosphinimide complexes." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/NQ62262.pdf.

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8

Scouter, Philip F. "Molecular compounds of the heavier Group 13 elements." Thesis, University of Oxford, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.308610.

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9

Tun, Zin-MIn. "Interactions of Group 13 Lewis Acids with Hexachlorocyclotriphosphazene." University of Akron / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=akron1226945430.

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10

Bauer, Tobias [Verfasser], and Rhett [Akademischer Betreuer] Kempe. "Group 3 and Group 13 Metal Hydride Compounds / Tobias Bauer. Betreuer: Rhett Kempe." Bayreuth : Universität Bayreuth, 2013. http://d-nb.info/105935263X/34.

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Книги з теми "Group 13"

1

W, Roesky H., and Atwood David A. 1965-, eds. Group 13 chemistry. Berlin: Springer, 2002.

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2

Shapiro, Pamela J., and David A. Atwood, eds. Group 13 Chemistry. Washington, DC: American Chemical Society, 2002. http://dx.doi.org/10.1021/bk-2002-0822.

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3

Roesky, Herbert W., and David A. Atwood, eds. Group 13 Chemistry I. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-47808-6.

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4

Roesky, Herbert W., and David A. Atwood, eds. Group 13 Chemistry II. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-45425-x.

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5

Roesky, Herbert W., and David A. Atwood, eds. Group 13 Chemistry III. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/3-540-46110-8.

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6

Japan) RIMS Workshop "Geometry of Transformation Groups and Combinatorics" (2011 Kyoto. Geometry of transformation groups and combinatorics: June 13-17, 2011. Kyoto, Japan: Research Institute for Mathematical Sciences, Kyoto University, 2013.

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7

Moi, Delphine, 13 ans. Paris: Pocket Jeunesse, 2004.

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8

Cannadine, Jason Christopher. Development of group 13 organometallic complexes for acrylate polymerisation. [s.l.]: typescript, 1994.

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9

Hardesty-Crouch, Brian. Holy things for youth ministry: 13 practical lessons. Cleveland: Pilgrim Press, 2010.

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10

Sastry, N. S. Narasimha, and Manoj Kumar Yadav, eds. Group Theory and Computation. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-13-2047-7.

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Частини книг з теми "Group 13"

1

Rankin, Hollie. "Group work." In Guide to Supporting Children through Bereavement and Loss, 43–51. Abingdon, Oxon ; New York, NY : Routledge, 2019.: Routledge, 2019. http://dx.doi.org/10.4324/9780429433160-13.

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2

Thomas, David N. "Journey into the Acting Community: Experiences of Learning and Change in Community Groups*." In Group Work, 167–81. London: Routledge, 2021. http://dx.doi.org/10.4324/9781003202097-13.

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3

Réaume, Denise. "Individuals, Groups, and Rights to Public Goods†." In Group Rights, 171–97. London: Routledge, 2022. http://dx.doi.org/10.4324/9781315253770-13.

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4

Berg, Robert C., Garry L. Landreth, and Kevin A. Fall. "Group Counseling with Adolescents." In Group Counseling, 181–90. Sixth edition. | New York : Routledge, 2017.: Routledge, 2017. http://dx.doi.org/10.4324/9781315157757-13.

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5

Tangolo, Anna Emanuela, and Anna Massi. "Monitoring group evolution through group imago analysis." In Group Therapy in Transactional Analysis, 105–19. London: Routledge, 2022. http://dx.doi.org/10.4324/9781003215547-13.

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6

Harrison, Larraine S. "Whole group drama." In Drama and Reading for Meaning Ages 4–11, 168–93. London: Routledge, 2022. http://dx.doi.org/10.4324/9781003250777-13.

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7

Clarke, Thomas. "HIH Insurance Group." In International Corporate Governance, 533–56. Second Edition. | New York : Routledge, 2017. | Revised edition of the author’s International corporate governance, 2007.: Routledge, 2017. http://dx.doi.org/10.4324/9781315749990-13.

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8

Berend, Kenrick, Gijsbert B. van der Voet, and Frederik A. de Wolff. "Acute Aluminum Intoxication." In Group 13 Chemistry II, 1–58. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-45425-x_1.

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9

Oshiro, Satoru. "A New Effect of Aluminum on Iron Metabolism in Mammalian Cells." In Group 13 Chemistry II, 59–77. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-45425-x_2.

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10

Anitha, Suram, and Kosagi Sharaf Jagannatha Rao. "The Complexity of Aluminum-DNA Interactions: Relevance to Alzheimer’s and Other Neurological Diseases." In Group 13 Chemistry II, 79–97. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-45425-x_3.

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Тези доповідей конференцій з теми "Group 13"

1

Cohn, Jeffrey F. "Beyond group differences." In MM '13: ACM Multimedia Conference. New York, NY, USA: ACM, 2013. http://dx.doi.org/10.1145/2512530.2512537.

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2

Okeke, Micheal, and Dong-Sheng Yang. "VIBRONIC SPECTRA OF GROUP 13 METAL-PIPERIDINE COMPLEXES." In 2021 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2021. http://dx.doi.org/10.15278/isms.2021.tl10.

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3

Abeles, Kim. "Shared Skies (13 global skies)." In SIGGRAPH '13: Special Interest Group on Computer Graphics and Interactive Techniques Conference. New York, NY, USA: ACM, 2013. http://dx.doi.org/10.1145/2503649.2503666.

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4

Jonas, Michael. "Group note taking in mediawiki, a collaborative approach." In SIGITE/RIIT'13: SIGITE/RIIT 2013. New York, NY, USA: ACM, 2013. http://dx.doi.org/10.1145/2512276.2512312.

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5

Williams, Helen, Liz Lewington, and Julie Kembrey. "P-13 The purple group – development of a parent-led bereavement group – the jessie may experience." In People, Partnerships and Potential, 16 – 18 November 2016, Liverpool. British Medical Journal Publishing Group, 2016. http://dx.doi.org/10.1136/bmjspcare-2016-001245.37.

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6

Wright, Ernest T., and David Ladd. "Apollo 13 views of the Moon in 4K." In SIGGRAPH '20: Special Interest Group on Computer Graphics and Interactive Techniques Conference. New York, NY, USA: ACM, 2020. http://dx.doi.org/10.1145/3368827.3389057.

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7

Feuerhake, Udo, and Monika Sester. "Mining group movement patterns." In SIGSPATIAL'13: 21st SIGSPATIAL International Conference on Advances in Geographic Information Systems. New York, NY, USA: ACM, 2013. http://dx.doi.org/10.1145/2525314.2525318.

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8

White, Langford B. "Radar signal synthesis with constraints: a group theoretic approach." In San Diego '90, 8-13 July, edited by Franklin T. Luk. SPIE, 1990. http://dx.doi.org/10.1117/12.23482.

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9

Renoust, Benjamin, Guy Melançon, and Marie-Luce Viaud. "Assessing group cohesion in homophily networks." In ASONAM '13: Advances in Social Networks Analysis and Mining 2013. New York, NY, USA: ACM, 2013. http://dx.doi.org/10.1145/2492517.2492619.

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10

Liu, Hong, Eugene Y. Vasserman, and Nicholas Hopper. "Improved group off-the-record messaging." In CCS'13: 2013 ACM SIGSAC Conference on Computer and Communications Security. New York, NY, USA: ACM, 2013. http://dx.doi.org/10.1145/2517840.2517867.

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Звіти організацій з теми "Group 13"

1

Bradley, E. R., P. G. Doctor, R. H. Ferris, and J. A. Buchanan. Steam generator group project: Task 13 final report: Nondestructive examination validation. Office of Scientific and Technical Information (OSTI), August 1988. http://dx.doi.org/10.2172/6815145.

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2

G. L. Schwendiman. Operable Unit 3-13, Group 3, Other Surface Soils (Phase II) Field Sampling Plan. Office of Scientific and Technical Information (OSTI), July 2006. http://dx.doi.org/10.2172/909337.

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3

L. Davison. Operable Unit 3-13, Group 3, Other Surface Soils (Phase I) Remedial Action Report. Office of Scientific and Technical Information (OSTI), July 2007. http://dx.doi.org/10.2172/917356.

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4

L. Davison. Operable Unit 3-13, Group 7, SFE-20 Hot Waste Tank System Remedial Action Request. Office of Scientific and Technical Information (OSTI), June 2009. http://dx.doi.org/10.2172/969280.

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5

Lee Davison. Operable Unit 3-13, Group 7, SFE-20 Hot Waste Tank System Remedial Action Report. Office of Scientific and Technical Information (OSTI), June 2009. http://dx.doi.org/10.2172/961523.

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6

D. Shanklin. 2005 Annual Operations Report for INTEC Operable Unit 3-13, Group 1, Tank Farm Interim Action. Office of Scientific and Technical Information (OSTI), July 2006. http://dx.doi.org/10.2172/909860.

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7

D. E. Shanklin. 2006 Annual Operations Report for INTEC Operable Unit 3-13, Group 1, Tank Farm Interim Action. Office of Scientific and Technical Information (OSTI), February 2007. http://dx.doi.org/10.2172/912633.

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G. L. Schwendiman. Operable Unit 3-13, Group 3, Other Surface Soils Remediation Sets 4-6 (Phase II) Waste Management Plan. Office of Scientific and Technical Information (OSTI), July 2006. http://dx.doi.org/10.2172/909842.

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B. G. Meagher. Public Participation Plan for Waste Area Group 7 Operable Unit 7-13/14 at the Idaho National Laboratory Site. Office of Scientific and Technical Information (OSTI), July 2007. http://dx.doi.org/10.2172/912630.

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D. E. Shanklin. Operable Unit 3-13, Group 3, Other Surface Soils Remediation Sets 4-6 (Phase II) Remedial Design/Remedial Action Work Plan. Office of Scientific and Technical Information (OSTI), June 2006. http://dx.doi.org/10.2172/909336.

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