Relevant bibliographies by topics / Butyl phosphates

Contents

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

Academic literature on the topic 'Butyl phosphates'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Butyl phosphates"

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Sajiki, Hironao, Yoshinari Sawama, Shota Asai, Kazuho Ban, and Yasunari Monguchi. "Selective N-Monoalkylation of Amide Derivatives with Trialkyl Phosphates." Synlett 29, no. 03 (2017): 322–25. http://dx.doi.org/10.1055/s-0036-1591494.

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A highly selective and easily handled monoalkylation of primary amide derivatives by using trialkyl phosphates as alkylating reagents in cyclopentyl methyl ether (CPME) was developed. Various monoalkylated amide derivatives were efficiently synthesized by changing the alkyl moiety (e.g., methyl, ethyl, butyl, or benzyl) of the trialkyl phosphate. These phosphate reagents are relatively stable and easily available, and CPME is a useful solvent in process chemistry.
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Kim, Sung Soo, Yu Zhu, In Seok Oh, and Chang Gyeong Lim. "Reactions of benzyl methyl substituted-benzyl phosphites with tert-butyl hypochlorite: "balanced TS" validating reactivity/selectivity principle." Canadian Journal of Chemistry 76, no. 6 (1998): 836–42. http://dx.doi.org/10.1139/v98-081.

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Reactions of a series of several benzyl methyl substituted-benzyl phosphites with tert-butyl hypochlorite were investigated. The reactions produced phosphates, isobutene, alkyl chlorides, and benzyl chlorides via phosphonium chlorides as intermediates. Furthermore, the phosphates bearing a tert-butyl group underwent fragmentation to yield isobutene and another phosphates. Relative rates of formations of substituted benzyl and benzyl chloride (kY/kH) were measured at the temperatures (-20, 0, 20, 40°C). Logarithms of the rates (log kY/kH) were plotted against sigma + and 1/T, respectively. The
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Tanaka, Hidekazu, Keigo Ishida, Takeshi Okumiya, and Masahiko Murakami. "Preparation and exfoliation of layered titanium butyl phosphates." Colloid and Polymer Science 288, no. 14-15 (2010): 1427–33. http://dx.doi.org/10.1007/s00396-010-2280-0.

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Yoshida, Akihiro, and Koichi Mikami. "Dramatic Changeover of Regioselectivity in the Reduction of Propargylic Phosphates by Palladium(0)/SmI2/Proton Source System." Synlett 12, no. 12 (1997): 1375–76. http://dx.doi.org/10.1055/s-0032-1316827.

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Abstract Regiodivergent synthesis of allenes and acetylenes was established in the reduction of propargylic phosphates. The palladium(0)-catalyzed reduction of secondary propargylic phosphates with samarium(II) iodide gave allenes or acetylenes by tuning proton sources (tert-butyl alcohol or dimethyl L-tartrate).
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Sarkar, Subramee, A. Suresh, and N. Sivaraman. "Third phase formation behaviour of tris(2-methylbutyl) phosphate and tri-n-alkyl phosphates in the extraction of mineral acids and tetravalent metal ions." Radiochimica Acta 109, no. 8 (2021): 625–34. http://dx.doi.org/10.1515/ract-2021-1023.

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Abstract The formation of third phase is a detrimental phenomenon witnessed in the nuclear separation processes during the extraction of certain metal salts by an organic solution, which comprises of a neutral extractant, tri-n-butyl phosphate dispersed in a non-polar diluent, n-dodecane (n-C12H26). In the present work, a comparative analysis on the third phase formation behaviour of three trialkyl phosphates, TBP, its linear and branched higher homologues tri-n-amyl phosphate and tris(2-methylbutyl) phosphate (T2MBP), respectively, have been provided which will be useful for the identificatio
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Yaramapa, Hari Babu, Cirandur Suresh Reddy, Venugopal Maralla, and Pedaiahgari Vasugovardhana Reddy. "New 2-aryloxy Macroheterocyclic Phosphates." Journal of Chemical Research 2005, no. 9 (2005): 587–89. http://dx.doi.org/10.3184/030823405774308880.

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A new class of phosphorus macroheterocycles (4a–j) has been synthesised in two steps. The reaction of 1 mole of 3,4-diamino-1,2,5-oxadiazole (1) with 2 moles of aqueous formaldehyde gave a Schiff's base which subsequently underwent addition with 2 moles of 4-t-butylphenol in 1,4-dioxane, afforded N,N-bis-(5-t-butyl-2-hydroxybenzyl)furazan-3,4-diamine (2). Cyclisation of 2 in situ with various substituted aryl phosphorodichloridates (3a–j) in the presence of Et3N in THF afforded 13-membered macroheterocycles (4a–j) containing P, N, O and C in good yields.
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Cieśla, J. M., R. Stolarski, and D. Shugar. "Cyclic phosphates of some antiviral acyclonucleosides: relationship between conformation and substrate/inhibitor properties in some enzyme systems." Acta Biochimica Polonica 40, no. 2 (1993): 251–60. http://dx.doi.org/10.18388/abp.1993_4826.

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Solution conformations, and substrate/inhibitor properties towards several phosphodiesterases and other nucleolytic enzymes, have been investigated for the cyclic phosphates of various acyclonucleosides, some with known antiviral activity, including 9-[(1,3-dihydroxy-2-propoxy)methyl]guanine (DHPG) and its carbocyclic congener, 9-(3,4-dihydroxybutyl)guanine (DHBG),9-[4-hydroxy-2-(hydroxymethyl)- butyl]-guanine (2HM-HBG), and 9-(2,3-dihydroxypropyl)guanine (HPG). Conformations of the cyclic phosphate rings were derived from analysis of the 1H-1H and 1H-31P vicinal coupling constants in the 1H n
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Prabhat, Parimal, Ankita Rao, Vivekchandra G. Mishra, Dipti J. Shah, Pradeep Kumar, and Bhupinder S. Tomar. "Direct extraction of uranium from yellow cake and ore matrices using supercritical carbon dioxide." Radiochimica Acta 108, no. 10 (2020): 769–77. http://dx.doi.org/10.1515/ract-2020-0009.

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AbstractThe study demonstrates the accomplishment of single step, direct supercritical fluid carbon dioxide (SC CO2) dissolution and extraction of uranium from crude matrices viz. yellow cakes (>90%) and rock phosphate ores (70%) employing adducts of trialkyl phosphates and nitric acid, thus avoiding free acid usage and eliminating number of process steps. Rock phosphate ore was made amenable for supercritical fluid extraction (SFE) system by unique strategy of pyrohydrolytic removal of fluorine. Pressure and temperature conditions, which were found to influence uranium extraction efficienc
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Lesage, Denis, Henri Virelizier, Christophe K. Jankowski, and Jean Claude Tabet. "Identification of minor products obtained during radiolysis of tributylphosphate (TBP)." Spectroscopy 13, no. 4 (1997): 275–90. http://dx.doi.org/10.1155/1997/565194.

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The structure identification of the fraction of minor products obtained during radiolysis of tributylphosphate (TBP), the solvent used in reprocessing of nuclear fuel, is reported. These results were realised from the distillation residue of the EDIT loop. The primary radiolysis formed TBP radical dimerises and is transformed under oxidative nitric acid conditions into several butyl chains substituted hydroxy or nitro phosphates as well as alkylated TBP. The butyl chain hydroxylated phosphate is leading to ketones, ethers and O-ester derivatives. The structures were determined by tandem mass s
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Lugmair, Claus G., T. Don Tilley, and Arnold L. Rheingold. "Zinc Di(tert-butyl)phosphate Complexes as Precursors to Zinc Phosphates. Manipulation of Zincophosphate Structures." Chemistry of Materials 9, no. 1 (1997): 339–48. http://dx.doi.org/10.1021/cm9603821.

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Dissertations / Theses on the topic "Butyl phosphates"

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Rawcliffe, John. "Microwave assisted decomposition of tri-butyl phosphate in aqueous effluent-streams." Thesis, University of Central Lancashire, 2000. http://clok.uclan.ac.uk/7865/.

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An investigation into the microwave assisted remediation of organic containing aqueous solutions has been conducted. Tri-n-butyl phosphate (TBP), the nuclear thel reprocessing solvent, and its diluents, are known to be responsible for the formation of interfacial deposits (cruds) in the alkali solvent wash stage of the Purex process for reprocessing spent nuclear fuel. The presence of cruds in the process is managed by regular wash out and the collected cruds are separated from aqueous washings and stored. Chemical oxidation of the cruds is one way of destroying them. This project explored mic
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Tarico, Daniel Joseph 1965. "Dispersion of alumina powder in secondary butyl alcohol with a phosphate ester surfactant." Thesis, The University of Arizona, 1990. http://hdl.handle.net/10150/277307.

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Most ceramic articles are produced by first dispersing powders in a suitable liquid, forming the dispersion (by casting, molding, extrusion, etc.), drying and then firing the body to its final sintered state. It has been recognized that dispersion characteristics strongly affect the green body which in turn determines properties of fired ceramic, and recently, dispersion science has become quite important in the development of ceramics processes. In this thesis research, colloidal size alumina powder was dispersed in secondary butyl alcohol with a phosphate ester dispersant. Dispersions were p
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Blaylock, Charles Robert. "Statistical evidence for competing equilibria models in the system Tri-N-Butyl phosphate-nitric acid-water-diluent." Thesis, Georgia Institute of Technology, 1986. http://hdl.handle.net/1853/12030.

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Armbruster, Florian. "Darstellung bor- und phosphorhaltiger Ringe durch Reaktionen von Halogenboranen und -phosphanen mit Bis(tert.-butyl-methyl)ketazin." Doctoral thesis, [S.l.] : [s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=973984112.

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Mu, Junju. "Computer simulation study of third phase formation in a nuclear extraction process." Thesis, University of Manchester, 2017. https://www.research.manchester.ac.uk/portal/en/theses/computer-simulation-study-of-third-phase-formation-in-a-nuclear-extraction-process(a1ad2143-4fc4-41cf-84c5-e447eeb0b3a3).html.

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Third phase formation is an undesirable phenomenon during the PUREX process, which is a continuous liquid-liquid extraction approach for the reprocessing of uranium and plutonium from spent nuclear fuel. When third phase formation occurs, the organic extraction solution splits into two layers. The light upper layer, which is commonly named the light organic phase, contains a lower concentration of metal ions, tri-n-butyl phosphate (TBP) and nitric acids but is rich in the organic diluent. The heavy lower layer, which is commonly named the third phase, contains high concentrations of metal ions
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JAYASINGHE, MANORI I. "HEAVY-METAL-ION TRANSPORT IN NANOPOROUS SELECTIVE-MEMBRANES: THEORY AND EXPERIMENT." University of Cincinnati / OhioLINK, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1186764159.

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Chu, Chien-Hua, and 朱建華. "The study on the Extraction of Chromium(VI) From Aqueous Solution by Tri-n-butyl phosphate." Thesis, 1996. http://ndltd.ncl.edu.tw/handle/61261360651877699877.

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Armbruster, Florian [Verfasser]. "Darstellung bor- und phosphorhaltiger Ringe durch Reaktionen von Halogenboranen und -phosphanen mit Bis(tert.-butyl-methyl)ketazin / vorgelegt von Florian Armbruster." 2004. http://d-nb.info/973984112/34.

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Books on the topic "Butyl phosphates"

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Seihin Hyōka Gijutsu Kiban Kikō. Rinsan tori-n- buchiru =: Tri-n-butyl phosphate. Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2009.

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World Health Organization (WHO). Tri-n-butyl Phosphate. World Health Organization, 1991.

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Book chapters on the topic "Butyl phosphates"

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Bährle-Rapp, Marina. "PPG-25 Butyl Ether Phosphate." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_8395.

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Bährle-Rapp, Marina. "Sodium C13–15 Pareth-8 Butyl Phosphate." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_9510.

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White, Peter D. "Phosphopeptide synthesis." In Fmoc Solid Phase Peptide Synthesis. Oxford University Press, 1999. http://dx.doi.org/10.1093/oso/9780199637256.003.0011.

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Protein phosphorylation mediated by protein kinases is the principal mechanism by which eukaryotic cellular processes are modulated by external physiological stimuli. Phosphopeptides are essential tools for the study of this process, serving as model substrates for phosphatases, as antigens for the production of antibodies against phosphorylated proteins, and as reference compounds for determining their physical parameters. The development of methods for the production of phosphopeptides has consequently attracted considerable interest over the last few years, and these endeavours have yielded reliable procedures which have now made their synthesis routine. There are two strategies used currently for the preparation of phosphopeptides: the building block approach, in which pre-formed protected phosphoamino acids are incorporated during the course of chain assembly, and the global phosphorylation method, which involves post-synthetic phosphorylation of serine, threonine, or tyrosine side-chain hydroxyl groups on the solid support. The building block procedure is certainly the more straightforward of the two approaches and has now become, owing to the availability of suitably protected phosphoamino acids, the standard method for the routine production of phosphopeptides. For the side-chain protection of phosphotyrosine in Fmoc/tBu-based solid phase synthesis, methyl, benzyl, t-butyl, dialkylamino, and silyl groups have been employed. Of these, benzyl is most useful as it is the most convenient to introduce and is rapidly removed during the TFA-mediated acidolysis step. Only the mono-benzyl ester, Fmoc-Tyr(PO(OBzl)-OH)-OH 1, is available commercially; the dibenzyl ester offers no practical benefit as it undergoes mono-debenzylation in the course of the piperidine-mediated Fmoc deprotection reaction. Also available commercially is Fmoc-Tyr(PO3H2)-OH 2. This derivative, despite having no phosphate protection, appears to work well, particularly in the synthesis of small- to medium-sized phosphopeptides; although formation of the pyrophosphate 3 can be a problem in peptides containing adjacent Tyr(PO3H2) residues. Phosphate triesters of serine and threonine are not compatible with Fmoc/tBu chemistry as they undergo β-elimination when treated with piperidine, resulting in the formation of dehydroalanine and dehydoaminobutyric acid, respectively For this reason, it was long believed that the building block approach could not be used for preparation of peptides containing these amino acids.
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Benkoski, Léa, and Tristan H. Lambert. "Construction of Multiple Stereocenters." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0039.

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Erick M. Carreira at ETH Zürich reported (Science 2013, 340, 1065) the enantiose­lective α-allylation of aldehyde 1 with alcohol 2 to produce 3 using a dual catalytic system involving a chiral iridium complex and amine 5. This stereodivergent method allows access to all of the possible stereoisomers of 3. In a conceptually related proc­ess, John F. Hartwig at the University of California, Berkeley reported (J. Am. Chem. Soc. 2013, 135, 2068) the highly stereoselective allylic alkylation of azlactone 6 with allylic carbonate 7 catalyzed by a combination of Ir(cod)Cl₂, ligand 9, and racemic silver phosphate 10. An enantioselective three-component Mannich-type reaction of tert-butyl diazo­acetate, aniline, and imine 11 to produce α,β-bis(arylamino) acid derivative 13 under dual catalysis with Rh₂(OAc)₄ and acid 12 was developed (Synthesis 2013, 45, 452) by Wenhao Hu at the Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development. Keiji Maruoka at Kyoto University reported (Chem. Commun. 2013, 49, 1118) a one-pot cross double-Mannich reaction of acetylalde­hyde 14, and imines 16 and 17 using axially chiral amino sulfonamide 15 to obtain densely functionalized 1,3-diamine 18 as a single stereoisomer. Jeffrey S. Johnson at the University of North Carolina at Chapel Hill reported (Org. Lett. 2013, 15, 2446) the asymmetric synthesis of enantioenriched anti-α-hydroxy-β-amino acid derivative 21 from 19 by treatment with oxone followed by catalytic hydrogenation using Ru(II) complex 20. Naoya Kumagai and Masakatsu Shibasaki at the Institute of Microbial Chemistry found (Org. Lett. 2013, 15, 2632) that a sil­ver complex of bisphosphine 24 effected a syn-selective and highly enantioselective Mannich-type reaction of aldimine 22 and α-sulfanyl lactone 23 to furnish the stereo­diad 25 with very high ee. The enantioselective homocrotylation of octanal 26 with cyclopropylcarbinylbo­ronate 27 to produce alcohol 28 with high ee was disclosed (J. Am. Chem. Soc. 2013, 135, 82) by Isaac J. Krauss at Brandeis University with computational studies pro­vided by Kendall N. Houk at UCLA. Benjamin List at the Max-Planck-Institut für Kohlenforschung reported (J. Am. Chem. Soc. 2013, 135, 6677) the enantioselective epoxidation of cyclohexenone 29 utilizing cinchona alkaloid- derived catalyst 30.
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Conference papers on the topic "Butyl phosphates"

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Piët, M. P. J., S. Chin, A. M. Prince, and B. Horowitz. "INACTIVATION OF VIRUSES IN PLASMA ON TREATMENT WITH TRI(N-BUTYL) PHOSPHATE (TNBP) DETERGENT MIXTURES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644149.

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Treatment of plasma with organic solvent/ detergent mixtures at the time of plasma collection or plasma pooling could reduce the exposure of technical staff to infectious virus and enhance the viral safety of final product. Treatment of plasma for 4 hours with 2% TNBP at 37°C or with 1% TNBP and 1% Tween 80 or Triton X-45 at 30°C resulted in the rapid and complete inactivation of ≥104 tissueculture infectious doses (TCID-50) ofvesicularstomatitis and Sindbis viruses, used as surrogates. TNBP and TNBP/Tween treatment of plasma was shown to inactivate ≥104 TCID-50 of human immunodeficiency virus
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Suleymanli, Khagani, Duygu Uysal, Rena Hamidova, et al. "Heat Capacity and Speed of Sound of 1-Butyl-3- Methylimidazolium Hex-afluoro¬phosphate and 1-Butyl-3- Methylimidazolium Trifluoro-Methanesulfonate Over Wide Range of Temperature." In 10TH International Conference on Sustainable Energy and Environmental Protection. University of Maribor Press, 2017. http://dx.doi.org/10.18690/978-961-286-064-6.4.

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Taylor, Robin J. "The Interactions of Iron and Plutonium Ions in Nitric Acid/Tri-Butyl Phosphate Systems and Process Flowsheets." In PLUTONIUM FUTURES - THE SCIENCE: Third Topical Conference on Plutonium and Actinides. AIP, 2003. http://dx.doi.org/10.1063/1.1594544.

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Hook, Adam, W. Neeyakorn, Jacqueline Krim, and Michael T. Dugger. "A Study of the Tribological Properties of Bound Plus Mobile Phase Lubricants With QCM and MEMS Sidewall Tribometers." In World Tribology Congress III. ASMEDC, 2005. http://dx.doi.org/10.1115/wtc2005-63676.

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Long chain alkylsilane monolayers used in the release process to protect MEMS devices from adhesion due to water adsorption also provide a very low coefficient of friction. One such monolayer, perfluorodecyltrichlorosilane (PFTS) has been shown to have very good thermal stability, keeping a water contact angle above 100° in air up to 400°C. [1] The monolayer will however wear under mechanical rubbing, causing the MEMS device to irreversibly adhere rendering it useless. Vapor phase lubricants (VPL) used in conjunction with self-assembled monolayers. may be the key to extending the life of rubbi
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Aperador, R., R. Navarro, G. Navio, and J. Acosta. "PREPARATION AND CHARACTERISTIC OF A F-IX CONCENTRATE TREATED WITH TRI-(N-BUTYL) PHOSPHATE (TNBP) AND TWEEN-80." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644847.

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This paper describes a method of preparation of F-IX concentrate, which uses 0,3% TNBP and 1% Tween-80,6 h, treatment to reduce the risk of transmitting viruses. The treated material was batch wise adsorbed on DEAE-Sephadex, washed and the F-IX concentrate was eluted with buffer on higher ionic strenghtWe have tested the effect of TNBP/Tween 80 treatment on the activity of coagulation factors as well as on trombogenicity, molecular filtration, and immunological assays
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Kelley, Dennis. "Proven Technologies for the Solidification of Complex Liquid Radioactive Waste (LRW): Global Case Studies of Applications and Disposal Options." In 2017 25th International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/icone25-66081.

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Legacy radioactive waste streams from the Cold War still exist and newly generated waste streams from nuclear power plants and research institutes go untreated and expose environmental hazards at many nuclear sites. The nature of the waste is extremely diverse, depending upon the source or the process from which it originated. The most problematic waste streams include complex liquids such as organic (tri-butyl-phosphate TBP) solutions contaminated with Pu and U isotopes, mixed sludge types, high acid radioactive waste, H-3 tritium contaminated organic and aqueous streams, etc. Environmental a
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Horowtz, M. S., M. W. Hilgartner, R. A. Lipton, C. Rooks, and B. Horowitz. "VIRAL SAFETY OF SOLVENT/DETERGENT-TREATED AHF IN PATIENTS WITH HEMOPHILIA." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644151.

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The safety of an Antihemophilic Factor concentrate (Factor VIII-SD) treated with the organic solvent tri(n-butyl) phosphate (TNBP) and sodium cholate is being assessed with respect to transmission of non-A, non-B hepatitis virus (NANBHV) and human immunodeficiency virus (HIV). TNBP/cholate treatment has been previously shown to inactivate at least 10,000 infectious doses each of hepatitis B virus (HBV) and NANBHV using a chimpanzee model, and 30,000 tissue culture infectious doses of HIV.Patients enrolled in the study have had no previous exposure to blood products made from plasma pools, alth
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Baumgartner, C., B. A. Perret, E. Meili, M. Furlan, H. Friedli, and J. J. Morgen-thaler. "NORMAL IN VIVO KINETICS OF FACTOR VIII (F VIII) AND FACTOR IX (F IX) TREATED WITH TRI (N-BUIYL) PHOSPHATE (TNBP) AND TWEEN 80 FOR INACTIVATION OF VIRUSES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644068.

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Heat treatment has been cxxnmonly used for the sterilisation of coagulation factor concentrates. This causes, however, considerable loss of coagulation factor activity? therefore alternative methods have been developed. Two new virus-inactivated coagulation factor preparations were recently introduced by our institution. Their manufacturing procedure includes a lipid solvent extraction step: The cryoprecipitate (F VIII preparation) or the first DEAE eluate (F IX preparation) is incubated with 0.3 % TNBP and 1 % Tveen 80 at 24°C for at least 12 hours. (Horowitz, Transfusion 25 : 516-522, 1985).
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Pokhitonov, Yury, Vasiliy Babain, Vladislav Kamachev, and Dennis Kelley. "Russia: Results and Prospects of Liquid Solidification Experiments at ROSATOM Sites." In ASME 2011 14th International Conference on Environmental Remediation and Radioactive Waste Management. ASMEDC, 2011. http://dx.doi.org/10.1115/icem2011-59112.

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Ongoing experimental work has been underway at selected nuclear sites in the Russian State Atomic Energy Corporation (ROSATOM) during the past two years to determine the effectiveness, reliability, application and acceptability of high technology polymers for liquid radioactive waste solidification. The long term project is funded by the U.S. Department of Energy’s Initiatives for Proliferation Prevention (IPP) program. IPP was established in 1994 as a non-proliferation program of DOE / National Nuclear Security Administration and receives its funding each year through Congressional appropriat
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Reports on the topic "Butyl phosphates"

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Siler, J. L. Reverse osmosis performance with solutions containing tri-n-butyl phosphate. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/10137084.

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Siler, J. L. Reverse osmosis performance with solutions containing tri-n-butyl phosphate. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/6645407.

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Rudisill, T. S. Initiation Temperature for Runaway Tri-n-Butyl Phosphate/Nitric Acid Reaction. Office of Scientific and Technical Information (OSTI), 2000. http://dx.doi.org/10.2172/768556.

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Hyder, M. L. Safe conditions for contacting nitric acid or nitrates with tri-n-butyl phosphate (TBP). Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10188417.

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Zamecnik, J. R. Evaluating the Effects of Tri-Butyl Phosphate and Normal Paraffin Hydrocarbon in Simulated Low-Activity Waste Solution on Ultrafiltration. Office of Scientific and Technical Information (OSTI), 2002. http://dx.doi.org/10.2172/801927.

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Adu-Wusu, K. Evaluating the Effects of Tri-Butyl Phosphate and Normal Paraffin Hydrocarbon in Simulated Low-Activity Waste Solution on Ion Exchange. Office of Scientific and Technical Information (OSTI), 2003. http://dx.doi.org/10.2172/810988.

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de Almeida, Valmor, Joseph F. Birdwell Jr, David W. DePaoli, and Costas Tsouris. Microflow Visualization of Tri-n-butyl-Phosphate/Dodecane and Nitric Acid in a Centrifugal Contactor. Part I: Flow Regimes, Transitions and Hysteresis. Office of Scientific and Technical Information (OSTI), 2017. http://dx.doi.org/10.2172/1410927.

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Barnes, M. J. The Effect of Tri-N-Butyl Phosphate on Tank 48 as a Result of Salt Solution Transfers within the In-Tank Precipitation Facility. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/292673.

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You might also be interested in the extended bibliographies on the topic 'Butyl phosphates' for particular source types:
Journal articles
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