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Thematische Bibliographien / Aqueous and non-aqueous systems

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Zeitschriftenartikel
Dissertationen
Bücher
Buchteile
Konferenzberichte
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Auswahl der wissenschaftlichen Literatur zum Thema „Aqueous and non-aqueous systems“

Autor: Grafiati

Veröffentlicht am 18. Mai 2024

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Zeitschriftenartikel zum Thema "Aqueous and non-aqueous systems"

1

Dyab, Amro K. F., und Hafiz N. Al-Haque. „Particle-stabilised non-aqueous systems“. RSC Advances 3, Nr. 32 (2013): 13101. http://dx.doi.org/10.1039/c3ra42338g.

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Friberg, Stig E. „Foams from non-aqueous systems“. Current Opinion in Colloid & Interface Science 15, Nr. 5 (Oktober 2010): 359–64. http://dx.doi.org/10.1016/j.cocis.2010.05.011.

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Kolker, A. R. „Thermodynamic modelling of concentrated aqueous electrolyte and non-aqueous systems“. Fluid Phase Equilibria 69 (Dezember 1991): 155–69. http://dx.doi.org/10.1016/0378-3812(91)90031-2.

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Sakthivel, Thiagarajan, Vikas Jaitely, Nisha V. Patel und Alexander T. Florence. „Non-aqueous emulsions: hydrocarbon–formamide systems“. International Journal of Pharmaceutics 214, Nr. 1-2 (Februar 2001): 43–48. http://dx.doi.org/10.1016/s0378-5173(00)00629-3.

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Binks, B. P., C. A. Davies, P. D. I. Fletcher und E. L. Sharp. „Non-aqueous foams in lubricating oil systems“. Colloids and Surfaces A: Physicochemical and Engineering Aspects 360, Nr. 1-3 (Mai 2010): 198–204. http://dx.doi.org/10.1016/j.colsurfa.2010.02.028.

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Mazzini, Virginia, und Vincent S. J. Craig. „Specific-ion effects in non-aqueous systems“. Current Opinion in Colloid & Interface Science 23 (Juni 2016): 82–93. http://dx.doi.org/10.1016/j.cocis.2016.06.009.

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Browarzik, D. „Phase-equilibrium calculations for non-aqueous and aqueous associating systems using continuous thermodynamics“. Fluid Phase Equilibria 230, Nr. 1-2 (März 2005): 143–52. http://dx.doi.org/10.1016/j.fluid.2004.12.006.

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Grace, Agbizu Cookey, und Ozioma Uzoma Daniel. „Micellization of a Cationic Surfactant in Mixed Aqueous and Non-aqueous Solvent Systems“. Journal of Applied Sciences and Environmental Management 19, Nr. 4 (29.02.2016): 577. http://dx.doi.org/10.4314/jasem.v19i4.2.

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Alaei, Zahra, Beatrice Cattoz, Peter John Dowding und Peter Charles Griffiths. „Solvent Relaxation NMR as a Tool to Study Particle Dispersions in Non-Aqueous Systems“. Physchem 2, Nr. 3 (15.07.2022): 224–34. http://dx.doi.org/10.3390/physchem2030016.

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The determination of the NMR spin–spin relaxation rate of water in (purely) aqueous particulate dispersions has been shown to be a convenient and facile experimental approach to probing the composition of near particle surface structures. Here, a systematic study has been undertaken of both non-aqueous and mixed aqueous–non-aqueous solvent particulate dispersions to explore the universality of the solvent relaxation technique. As in the aqueous case, a linear relationship between the surface area present and the solvent relaxation rate is observed, confirming the rapid exchange of the solvent molecules between the surface and the bulk and thereby illustrating the viability of the experimental methodology to study such systems. Crucially, the surface enhancement effect was considerably weaker in non-aqueous systems compared with aqueous dispersions and reflects a potential limitation of the wider deployment of this experimental methodology.

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Wang, Jiping, Yuanyuan Gao, Lei Zhu, Xiaomin Gu, Huashu Dou und Liujun Pei. „Dyeing Property and Adsorption Kinetics of Reactive Dyes for Cotton Textiles in Salt-Free Non-Aqueous Dyeing Systems“. Polymers 10, Nr. 9 (15.09.2018): 1030. http://dx.doi.org/10.3390/polym10091030.

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In recent years, new concepts in textile dyeing technology have been investigated which aim to decrease the use of chemicals and the emission of water. In this work, dyeing of cotton textiles with reactive dyes has been investigated in a silicone non-aqueous dyeing system. Compared with conventional aqueous dyeing, almost 100% of reactive dyes can be adsorbed on cotton textiles without using any salts in non-aqueous dyeing systems, and the fixation of dye is also higher (80%~90% for non-aqueous dyeing vs. 40%~50% for traditional dyeing). The pseudo-second-order kinetic model can best describe the adsorption and equilibrium of reactive dyes in the non-aqueous dyeing systems as well as in the traditional water dyeing system. In the non-aqueous dyeing systems, the adsorption equilibrium of reactive dyes can be reached quickly. Particularly in the siloxane non-aqueous dyeing system, the adsorption equilibrium time of reactive dye is only 5–10 min at 25 °C, whereas more time is needed at 60 °C in the water dyeing system. The surface tension of non-aqueous media influences the adsorption rate of dye. The lower the surface tension, the faster the adsorption rate of reactive dye, and the higher the final uptake of dye. As a result, non-aqueous dyeing technology provides an innovative approach to increase dye uptake under a low dyeing temperature, in addition to making large water savings.

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Dissertationen zum Thema "Aqueous and non-aqueous systems"

1

Smylie, J. „Studies on the mechanism of template polymerisation in aqueous and non-aqueous systems“. Thesis, University of Strathclyde, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.372123.

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Jayaraman, Krithika M. „Mass transfer from non-aqueous phase liquids to the aqueous phase in groundwater systems“. Thesis, This resource online, 1992. http://scholar.lib.vt.edu/theses/available/etd-01122010-020214/.

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Banerjee, Ashis. „Rheological and thermodynamic investigation of some properties prevailing in aqueous and non-aqueous system“. Thesis, University of North Bengal, 2009. http://hdl.handle.net/123456789/1357.

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Al-Dulaimi, Zaid. „Non-aqueous shale gas recovery system“. Thesis, Cardiff University, 2017. http://orca.cf.ac.uk/104172/.

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gh European energy demands, the difference in prices amongst Europe and ambitious gas producers, have produced a scenario of high competition in a region that suffers a lack of fossil resources still required for energy generation. Therefore, other sources are under the scope of various countries to mitigate these issues. Shale gas is one fuel that presents a scenario that would decrease European dependence on imported gas. Although shale gas production is unlikely to give the energy security desired to the whole Europe, it would make a difference for the communities that will adopt it. However, shale gas has acquired a bad reputation with the public, mainly because of its extraction methods. This bad reputation is attributed to hydraulic fracturing, technology well-known as fracking, and its risks associated towards air and water pollution. Therefore, companies, institutions and governments are looking for other alternative methods of extraction with more environmentally friendly processes. Producing extensive high-pressure pulse waves at the base of the wellbore by using detonation is a promising potential technique for shale gas extraction. A fundamental study of deflagration to detonation transition using recirculated shale gas formation with pure oxygen as an oxidiser has been studied to design a system with lower DDT distance and higher pressure waves. Three proposed cases of UK shale gas composition were studied. Chemical equilibrium software GASEQ and chemical kinetic software CHEMKIN-PRO were used to estimate the product parameters. Results showed that the effect produced by diluents, such as carbon dioxide, are eliminated by the use of higher hydrogen content carbon-to-hydrogen species for the three cases proposed. OpenFOAM CFD was used to calculate the deflagration to detonation transition parameters in stoichiometric hydrogen air mixtures to evaluate different obstacle geometries on the transition phenomenon to improve the detonation process. The shape and layout of obstacles were found to have a significant effect on flame acceleration, and subsequent detonation propagation. The interaction of transverse pressure waves generated at the obstructions governs the propagation mechanism. The transverse waves and its frequency appear to play a pivotal role in supporting the detonation wave. H iv It was found that rectangular shape obstacles reduce the reaction time, while triangular ones achieved detonation with the minimum run-up distance. On the other hand, semicircular shape obstacles generate the highest pressure in a detonation tube. The outcome from numerical calculations and CFD were the guide to construct an experimental rig of 21.2mm diameter and 1500mm length tube with different obstacle configurations to demonstrate the concept of pulse detonation for shale rock cracking. Experimental work has been performed to determine the potential of shale gas production in the Dullais Valley, South of Wales. It was found through several tests using BS standard volatile analyses, Transmission Electron Microscopy and pyrolysis RockEval evaluation that the potential of extraction in this region is fair, with similar concentrations of pyrite but with low energy content compared to those resources located in the Midlands and Yorkshire. However, the use of controlled pulse detonation could be the ideal technology for extraction in Wales, as low sulphur (S) content will produce lower unwanted emissions, with a process that can promote opening of pores and further gasification of oil based molecular, with a subsequent increase in shale gas production, topic that requires further research. Finally, a 2-dimensional simulation was performed using ANSYS Parameter Design Language (APDL) to investigate the effect of pressure pulse generated by the detonation tube on a pre-crack. Results showed that the layer close to the applied load will be displaced, which means that it will be smashed. The maximum Von Mises stresses were found to concentrate at the perforating hole corners, while the region immediately after the crack tip is susceptible to compression stresses. The Same behaviour was found for the stress intensity factor. According to that, it is believed that the cracks will propagate diagonally from the perforating hole base. Therefore, the current work has theoretically demonstrated the technology for shale gas recovery, with an optimised geometry consistent of internal obstacles, for a region with potential for shale gas exploitation.

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Dakua, Vikas Kumar. „Physico-chemical studies on interactions between ion-solvent, ion-ion and solvent-solvent in aqueous and non-aqueous pure and mixed solvent systems“. Thesis, University of North Bengal, 2008. http://hdl.handle.net/123456789/707.

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Das, Samir. „Investigation of solution behaviour and inclusion complexation of some noteworthy compounds with the manifestation of assorted interactions prevalent in aqueous and non-aqueous systems“. Thesis, University of North Bengal, 2022. http://ir.nbu.ac.in/handle/123456789/4788.

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Escalante, García Ismailia Leilani. „Fundamental and Flow Battery Studies for Non-Aqueous Redox Systems“. Case Western Reserve University School of Graduate Studies / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=case1425046485.

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Theaker, Ian. „A structural and thermodynamic study of non-aqueous solvent/wax systems“. Thesis, University of Hull, 1996. http://hydra.hull.ac.uk/resources/hull:4996.

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Non-aqueous wax/solvent systems of industrial relevance for the manufacture of paste polishes have been investigated. These mixtures have been modelled using a paraffin wax of Japanese origin (Nippon Seiro 140/145°F) in a solution of pure heptane to which dopant components are added.The stability of any resulting gel has been assessed via solubility studies and measurement of the solvent vapour pressure. A new technique for the measurement of vapour pressure in these systems has been developed. The operation of the apparatus has been made almost completely automatic by the use of modern control units.Complementary analytical techniques such as Differential Scanning Calorimetry and Nuclear Magnetic Resonance have been used to augment the data where appropriate and the structure of these pastes has been investigated with the use of Optical Microscopy.

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Islam, Mojahedul. „The stability of foam, with special emphasis on non-aqueous systems“. Thesis, Imperial College London, 1987. http://hdl.handle.net/10044/1/46269.

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Templeton, John Andrew. „Magnetite Oxidation in Aqueous Systems“. Thesis, Virginia Tech, 2008. http://hdl.handle.net/10919/43468.

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Magnetite, an iron oxide, is a possible candidate for in situ remediation of contaminated groundwater systems due to its oxidation/reduction potential for reduction of contaminants such as carbon tetrachloride. Little characterization and analysis has been done to describe the kinetics of magnetite transformation during oxidation. This work focuses on monitoring the concentrations of magnetite and one of its oxidation transformation products, maghemite, by the use of UV-Vis-NIR spectroscopy. As oxidation proceeded at a constant specific temperature, the concentration of magnetite decreases, which was indicated by a decrease in absorption in the NIR-region of the spectrum. As magnetite concentrations decreased, the concentration of maghemite increased, which was indicated by an increase in absorption in the UV-region. The temperature at which the suspensions of magnetite and maghemite were measured was of great importance for complete understanding of the magnetite transformation as seen by UV-Vis-NIR spectroscopy analysis. Higher measurement temperatures produced higher absorptivities of FeII-FeIII electron hopping transitions, while decreasing the absorptivity of FeIII-FeIII in the NIR and UV-regions respectively. Lower temperatures produced the opposite effects on the iron oxidesâ transitions. Higher temperature increased the rate of oxidation.
Master of Science

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Bücher zum Thema "Aqueous and non-aqueous systems"

1

Hatti-Kaul, Rajni. Aqueous Two-Phase Systems. New Jersey: Humana Press, 2000. http://dx.doi.org/10.1385/1592590284.

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Anghel, Dan F., Hrsg. Aqueous Polymer — Cosolute Systems. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/3-540-36114-6.

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Cristiano, Poleto, und Charlesworth Susanne, Hrsg. Sedimentology of aqueous systems. Hoboken, NJ: Wiley, 2010.

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Sedimentology of aqueous systems. Hoboken, NJ: Wiley, 2010.

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Fisher, Derek, und Ian A. Sutherland, Hrsg. Separations Using Aqueous Phase Systems. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4684-5667-7.

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Melchior, Daniel C., und R. L. Bassett, Hrsg. Chemical Modeling of Aqueous Systems II. Washington, DC: American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0416.

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Freire, Mara G., Hrsg. Ionic-Liquid-Based Aqueous Biphasic Systems. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-52875-4.

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1958-, Melchior Daniel C., Bassett R. L. 1948-, American Chemical Society. Division of Geochemistry. und American Chemical Society Meeting, Hrsg. Chemical modeling of aqueous systems II. Washington, DC: American Chemical Society, 1990.

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Moreno-Piraján, Juan Carlos. Thermodynamics: Physical chemistry of aqueous systems. Rijeka, Croatia: InTech, 2011.

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Ferraris, Giovanni, M. Prieto und H. Stoll, Hrsg. Ion Partitioning in Ambient-Temperature Aqueous Systems. London: Mineralogical Society of Great Britain & Ireland, 2011. http://dx.doi.org/10.1180/emu-notes.10.

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Buchteile zum Thema "Aqueous and non-aqueous systems"

1

Waks, Marcel. „Enzymes in Non-Aqueous Systems“. In The Enzyme Catalysis Process, 465–75. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-1607-8_30.

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Bosley, John A., und Alan D. Peilow. „Immobilization of Lipases for Use in Non-Aqueous Reaction Systems“. In Methods in Non-Aqueous Enzymology, 52–69. Basel: Birkhäuser Basel, 2000. http://dx.doi.org/10.1007/978-3-0348-8472-3_4.

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Anthonsen, Thorleif, und Birte J. Sjursnes. „Importance of Water Activity for Enzyme Catalysis in Non-Aqueous Organic Systems“. In Methods in Non-Aqueous Enzymology, 14–35. Basel: Birkhäuser Basel, 2000. http://dx.doi.org/10.1007/978-3-0348-8472-3_2.

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Van Bael, Marlies K., An Hardy und Jules Mullens. „Aqueous Precursor Systems“. In Chemical Solution Deposition of Functional Oxide Thin Films, 93–140. Vienna: Springer Vienna, 2013. http://dx.doi.org/10.1007/978-3-211-99311-8_5.

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Silberberg, A. „Gelled Aqueous Systems“. In Polymers in Aqueous Media, 3–14. Washington, DC: American Chemical Society, 1989. http://dx.doi.org/10.1021/ba-1989-0223.ch001.

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Berge, Philippe. „Modelling Corrosion in Nuclear Systems“. In Modelling Aqueous Corrosion, 65–87. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1176-8_3.

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Roberge, P. R. „Expert Systems for Corrosion Prevention and Control“. In Modelling Aqueous Corrosion, 129–40. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1176-8_6.

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Save, Supriya S., und Sanjiv V. Save. „Mass Transfer in Aqueous Two-Phase Systems“. In Aqueous Biphasic Separations, 71–81. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4615-1953-9_6.

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Cunningham, Michael, Marcus Lin, Jodi-Anne Smith, John Ma, Kim McAuley, Barkev Keoshkerian und Michael Georges. „Nitroxide-mediated living radical polymerization in dispersed systems“. In Aqueous Polymer Dispersions, 88–93. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/b12144.

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Cunningham, Michael, Marcus Lin, Jodi-Anne Smith, John Ma, Kim McAuley, Barkev Keoshkerian und Michael Georges. „Nitroxide-mediated living radical polymerization in dispersed systems“. In Aqueous Polymer Dispersions, 88–93. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-540-36474-0_18.

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Konferenzberichte zum Thema "Aqueous and non-aqueous systems"

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Buller, J., und J. F. Carpenter. „H2S Scavengers for Non-Aqueous Systems“. In SPE International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 2005. http://dx.doi.org/10.2118/93353-ms.

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Li, Yibo, Tianshuang He, Jinzhou Zhao, Xiang Lin, Lin Sun, Bing Wei und Wanfen Pu. „Integrity Investigation of Macroscopic and Microscopic Properties of Non-Aqueous Foams for Enhanced Oil Recovery“. In International Petroleum Technology Conference. IPTC, 2023. http://dx.doi.org/10.2523/iptc-22922-ms.

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Abstract Foam flooding is a crucial enhanced oil recovery technique for profile control during the oil displacement process. The stability of the foam is the key factor for the success of foam flooding, but typical aqueous foams generally lose their stability in the presence of hydrocarbons because of their low oil tolerance. Non-aqueous foams possess outstanding stability in the presence of hydrocarbons as a result of their unique properties. However, few studies have been conducted on the stabilization mechanisms of non-aqueous foams in the presence of hydrocarbons. In this study, comparative experiments were performed to investigate differences in the stabilization mechanism between aqueous and non-aqueous foams. The results showed that a non-aqueous foam had excellent oil tolerance in a bulk foaming test. Then, the stabilization mechanisms of foams were investigated in terms of surface dilatational viscoelasticity and liquid film thinning. For a non-aqueous foam system, the maximum viscoelastic modulus of 55 mN/m occurred at a surfactant concentration of 5.0 wt%, which indicated that the foam was more stable. In a foam film thinning experiment, the thinning time of an aqueous foam system was shortened but the liquid film thickness was increased by crude oil, whereas crude oil increased the thinning time of a non-aqueous foam system but decreased its liquid film thickness. In a non-aqueous foam system, the film could remain stable for hours before rupturing, which indicated that its stability in the presence of an oil phase was excellent. These results are meaningful for the understanding of the stabilization mechanisms of oil-based foams and the employment of non-aqueous foams for enhanced oil recovery.

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Bloomingburg, G. F., J. M. Simonson, R. C. Moore, H. D. Cochran und R. E. Mesmer. „AQUEOUS ELECTROLYTE MODELING IN ASPEN PLUS“. In Physical Chemistry of Aqueous Systems: Meeting the Needs of Industry. Connecticut: Begellhouse, 2023. http://dx.doi.org/10.1615/icpws-1994.630.

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Cummings, P. T., H. D. Cochran und A. A. Chialvo. „MOLECULAR SIMULATION OF SUPERCRITICAL AQUEOUS SOLUTIONS“. In Physical Chemistry of Aqueous Systems: Meeting the Needs of Industry. Connecticut: Begellhouse, 2023. http://dx.doi.org/10.1615/icpws-1994.330.

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Mastiani, Mohammad, Seokju Seo, Sofia Melgar Jimenez, Nick Petrozzi und Myeongsub (Mike) Kim. „Understanding Fundamental Physics of Aqueous Droplet Generation Mechanisms in the Aqueous Environment“. In ASME 2017 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/imece2017-71542.

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Recent advent of Aqueous-Two-Phase-System (ATPS), more biologically friendly compared to conventional oil-water systems, has shown great potential to rapidly generate aqueous droplets without tedious post-processing. However, understanding of underlying physics of droplet formation in ATPS is still in its infancy. In this paper, we investigate hydrodynamic behaviors and mechanisms of all-aqueous droplet formation in two flow-focusing droplet generators. Two incompatible polymers namely polyethylene glycol (PEG) and dextran (DEX) are mixed in water to make ATPS. The influence of inlet pressures and flow-focusing configurations on droplet sizes, and thread breakup length is studied. Flow regime mapping for two different configurations of droplet generators possessing junction angles of 30° and 90° is also obtained. The results show that droplet size is very susceptible to the junction angle while inlet pressures of the PEG and DEX flows readily control four main flow regimes including back flow, dripping, jetting and stratified.

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LARIA, Daniel, und Roberto FERNANDEZ-PRINI. „IONS IN STEAM AND IN AQUEOUS CLUSTERS“. In Physical Chemistry of Aqueous Systems: Meeting the Needs of Industry. Connecticut: Begellhouse, 2023. http://dx.doi.org/10.1615/icpws-1994.620.

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Miles, A. F., O. Vikane, D. S. Healey, I. R. Collins, J. Saeten, H. M. Bourne und R. G. Smith. „Field Experiences Using ‘Oil Soluble' Non-Aqueous Scale Inhibitor Delivery Systems“. In SPE International Symposium on Oilfield Scale. Society of Petroleum Engineers, 2004. http://dx.doi.org/10.2118/87431-ms.

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Kriksunov, Leo B., und Digby D. Macdonald. „ADVANCES IN MEASURING CHEMISTRY PARAMETERS IN HIGH TEMPERATURE AQUEOUS SYSTEMS“. In Physical Chemistry of Aqueous Systems: Meeting the Needs of Industry. Connecticut: Begellhouse, 2023. http://dx.doi.org/10.1615/icpws-1994.550.

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Lvov, Serguei N., Giorgio Perboni und Maria Broglia. „HIGH TEMPERATURE pH MEASUREMENTS IN DILUTE AQUEOUS AMMONIA SOLUTIONS“. In Physical Chemistry of Aqueous Systems: Meeting the Needs of Industry. Connecticut: Begellhouse, 2023. http://dx.doi.org/10.1615/icpws-1994.560.

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Thompson, Nathaniel B., Christopher L. Tanner, John C. Gallon und Ashley C. Karp. „Pyrotechnically Actuated Gas Generator Utilizing Aqueous Methanol“. In 23rd AIAA Aerodynamic Decelerator Systems Technology Conference. Reston, Virginia: American Institute of Aeronautics and Astronautics, 2015. http://dx.doi.org/10.2514/6.2015-2115.

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Berichte der Organisationen zum Thema "Aqueous and non-aqueous systems"

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Smith, M. D., und G. W. Christoff. Environmentally conscious closed-loop aqueous and semi-aqueous cleaning systems for defluxing and degreasing. Office of Scientific and Technical Information (OSTI), März 1996. http://dx.doi.org/10.2172/212492.

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Nash, Ken, Leigh Martin und Gregg Lumetta. Advanced Aqueous Separation Systems for Actinide Partitioning. Office of Scientific and Technical Information (OSTI), April 2015. http://dx.doi.org/10.2172/1178435.

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Chaiko, D. J., B. Zaslavsky, A. N. Rollins, Y. Vojta, J. Gartelmann und W. Mego. Metal separations using aqueous biphasic partitioning systems. Office of Scientific and Technical Information (OSTI), Mai 1996. http://dx.doi.org/10.2172/231396.

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4

Nash, Kenneth L., Sue Clark, G. Patrick Meier, Spiro Alexandratos, Robert Paine, Robert Hancock und Dale Ensor. Advanced Aqueous Separation Systems for Actinide Partitioning. Office of Scientific and Technical Information (OSTI), März 2012. http://dx.doi.org/10.2172/1037326.

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5

Heaton, R. C., W. M. Jones und K. P. Coffelt. Plutonium release from radioisotope heat sources into aqueous systems. Office of Scientific and Technical Information (OSTI), Dezember 1989. http://dx.doi.org/10.2172/5191563.

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6

WOODHAM, WESLEY. THERMODYNAMICS OF DEUTERIUM OXIDE SEPARATIONS IN AQUEOUS TWO-PHASE SYSTEMS. Office of Scientific and Technical Information (OSTI), Oktober 2020. http://dx.doi.org/10.2172/1676414.

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7

Kingston, A. W., und O. H. Ardakani. Diagenetic fluid flow and hydrocarbon migration in the Montney Formation, British Columbia: fluid inclusion and stable isotope evidence. Natural Resources Canada/CMSS/Information Management, 2022. http://dx.doi.org/10.4095/330947.

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Annotation:

The Montney Formation in Alberta and British Columbia, Canada is an early Triassic siltstone currently in an active diagenetic environment at depths greater than 1,000 m, but with maximum burial depths potentially exceeding 5,000 m (Ness, 2001). It has undergone multiple phases of burial and uplift and there is strong evidence for multiple generations of hydrocarbon maturation/migration. Understanding the origin and history of diagenetic fluids within these systems helps to unravel the chemical changes that have occurred since deposition. Many cores taken near the deformation front display abundant calcite-filled fractures including vertical or sub-vertical, bedding plane parallel (beefs), and brecciated horizons with complex mixtures of vertical and horizontal components. We analyzed vertical and brecciated horizons to assess the timing and origin of fluid flow and its implications for diagenetic history of the Montney Fm. Aqueous and petroleum bearing fluid inclusions were observed in both vertical and brecciated zones; however, they did not occur in the same fluid inclusion assemblages. Petroleum inclusions occur as secondary fluid inclusions (e.g. in healed fractures and along cleavage planes) alongside primary aqueous inclusions indicating petroleum inclusions post-date aqueous inclusions and suggest multiple phases of fluid flow is recorded within these fractures. Raman spectroscopy of aqueous inclusions also display no evidence of petroleum compounds supporting the absence or low abundance of petroleum fluids during the formation of aqueous fluid inclusions. Pressure-corrected trapping temperatures (&gt;140°C) are likely associated with the period of maximum burial during the Laramide orogeny based on burial history modelling. Ice melt temperatures of aqueous fluid inclusions are consistent with 19% NaCl equiv. brine and eutectic temperatures (-51°C) indicate NaCl-CaCl2 composition. Combined use of aqueous and petroleum fluid inclusions in deeply buried sedimentary systems offers a promising tool for better understanding the diagenetic fluid history and helps constrain the pressure-temperature history important for characterizing economically important geologic formations.

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8

Pawel, S. J. A performance evaluation of coating systems for long term aqueous immersion service. Office of Scientific and Technical Information (OSTI), November 1994. http://dx.doi.org/10.2172/39125.

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9

Wolery, T. J., K. E. Robert, D. A. Wruck, A. Brachmann und C. E. A. Palmer. Combine Studies Pertaining to the Solubility of Neptunium in Oxidizing Aqueous Systems. Office of Scientific and Technical Information (OSTI), September 2000. http://dx.doi.org/10.2172/793680.

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10

Li, D. Bimetallic Porous Iron (pFe) Materials for Remediation/Removal of Tc from Aqueous Systems. Office of Scientific and Technical Information (OSTI), September 2017. http://dx.doi.org/10.2172/1395971.

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