Littérature scientifique sur le sujet « Solvent-solvent »
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Articles de revues sur le sujet "Solvent-solvent"
Zhou, Shi-Qi. « Influence of Solvent-Solvent and Solute-Solvent Interaction Properties on Solvent-Mediated Potential ». Communications in Theoretical Physics 44, no 2 (août 2005) : 365–70. http://dx.doi.org/10.1088/6102/44/2/365.
Texte intégralGrigorescu, Gabriela, Silvia Ioan et Bogdan C. Simionescu. « Solvent/solvent/polymer ternary systems ». Polymer Bulletin 31, no 1 (juillet 1993) : 123–27. http://dx.doi.org/10.1007/bf00298774.
Texte intégralChan, Joel, Joseph Chee Chang, Tom Hope, Dafna Shahaf et Aniket Kittur. « SOLVENT ». Proceedings of the ACM on Human-Computer Interaction 2, CSCW (novembre 2018) : 1–21. http://dx.doi.org/10.1145/3274300.
Texte intégralLuca, Alfio A. Tamburello, Philippe Hébert, Pierre F. Brevet et Hubert H. Girault. « Surface second-harmonic generation at air/solvent and solvent/solvent interfaces ». J. Chem. Soc., Faraday Trans. 91, no 12 (1995) : 1763–68. http://dx.doi.org/10.1039/ft9959101763.
Texte intégralda Silva, Domingas C., Ingrid Ricken, Marcos A. do R. Silva et Vanderlei G. Machado. « Solute-solvent and solvent-solvent interactions in the preferential solvation of Brooker's merocyanine in binary solvent mixtures ». Journal of Physical Organic Chemistry 15, no 7 (2002) : 420–27. http://dx.doi.org/10.1002/poc.519.
Texte intégralSouvignet, Isabelle, et Susan V. Olesik. « Solvent-Solvent and Solute-Solvent Interactions in Liquid Methanol/Carbon Dioxide Mixtures ». Journal of Physical Chemistry 99, no 45 (novembre 1995) : 16800–16803. http://dx.doi.org/10.1021/j100045a048.
Texte intégralVrentas, J. S., C. M. Vrentas et N. Faridi. « Effect of Solvent Size on Solvent Self-Diffusion in Polymer−Solvent Systems ». Macromolecules 29, no 9 (janvier 1996) : 3272–76. http://dx.doi.org/10.1021/ma9511356.
Texte intégralVillacampa, Manuel, Elena Diaz de Apodaca, Jose R. Quintana et Issa Katime. « Diblock Copolymer Micelles in Solvent Binary Mixtures. 2. Selective Solvent/Good Solvent ». Macromolecules 28, no 12 (juin 1995) : 4144–49. http://dx.doi.org/10.1021/ma00116a014.
Texte intégralKohl, Stephan W., Frank W. Heinemann, Markus Hummert, Walter Bauer et Andreas Grohmann. « Solvent dependent reactivity : solvent activation vs. solvent coordination in alkylphosphane iron complexes ». Dalton Transactions, no 47 (2006) : 5583. http://dx.doi.org/10.1039/b610792c.
Texte intégralYAMAGUCHI, T., et Y. KIMURA. « Effects of solute-solvent and solvent-solvent attractive interactions on solute diffusion ». Molecular Physics 98, no 19 (10 octobre 2000) : 1553–63. http://dx.doi.org/10.1080/00268970009483361.
Texte intégralThèses sur le sujet "Solvent-solvent"
Chun-Te, Lin Justin. « Organic solvent nanofiltration membrane cascades for solvent exchange and purification ». Thesis, Imperial College London, 2008. http://hdl.handle.net/10044/1/11977.
Texte intégralMęcfel-Marczewski, Joanna. « Self Incompatible Solvent ». Doctoral thesis, Universitätsbibliothek Chemnitz, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-201001195.
Texte intégralIn this thesis a new principle of Self Incompatible Solvent is introduced. It is shown theoretically that a preexisting mixture of two substances (compound 1 and 2) with unfavorable interactions will readily dissolve a third compound because it diminishes the unfavorable interaction between the compound 1 and 2 by dilution. This behavior should be the stronger the more unfavorable the interactions between compound 1 and 2 are. However, substances with strong unfavorable interactions will not mix. Therefore the idea pursued here is to enforce the desired preexisting mixture for example by linking compound 1 covalently to compound 2. Such a molecule that is composed of two incompatible parts is called Self Incompatible Solvent in this work. In this thesis examples of incompatible compounds that show moderate incompatibility are chosen, therefore it was possible to do a comparison between simple physical mixtures and covalently linked incompatible molecules. The theoretical prediction of the theory is compared with experiments. This principle is calculated quantitatively for binary and ternary mixtures and compared with the experimental results in three distinct series of experiments: i) by using solution calorimetry and calculation of the interaction parameters between compounds 3 and the preexisting binary mixture of compound 1 and 2, ii) by using solution calorimetry and calculation of the interaction parameters between compound 3 and the Self Incompatible Solvent that correspond to the mixtures used in (i) and iii) from the saturation solubility of compound 3 in the Self Incompatible Solvent. The results obtained from the theoretical prediction and these obtained from the three different series of experiments show the same trend: the self incompatibility of the solvent improves the dissolution process
Rodarte, Alma Isabel Marín. « Predispersed solvent extraction ». Thesis, Virginia Tech, 1988. http://hdl.handle.net/10919/45173.
Texte intégralA new solvent extraction method has been developed for the extraction of metal and organic ions from very dilute aqueous solutions. The new method, which has been named Predispersed Solvent Extraction (POSE), is based on the principle that 1 there is no need to comminute both phases. All that is necessary is to comminute the solvent phase prior to contacting it with the feed. This is done by converting the solvent into aphrons, which are micron-sized globules encapsulated in a soapy film. Since the aphrons are so small, it takes a long time for the solvent to rise to the surface under the influence of gravity alone. Therefore, the separation is expedited by piggy-back flotation of the aphrons on specially prepared gas bubbles, which are somewhat larger than aphrons and are called colloidal gas aphrons (CGA).
Copper, uranium and chromium ions, and alizarin yellow were extracted from very dilute aqueous solutions using PDSE. Tests were performed in a vertical glass column in both batch and continuous modes, and in a continuous horizontal trough. The new solvent extraction procedure worked very efficiently and very quickly under laboratory conditions. Higher than 99% extraction was achieved in many of the tests performed.
Master of Science
Xu, Zhuang. « PARTITIONING OF SOLVENT MOLECULES SURROUNGDING POLYMER CHIANS IN SOLVENT-SHIFTING PROCESS ». University of Akron / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=akron1555690517286259.
Texte intégralWang, Nan. « CO2 Separation - from Aqueous Amine Solvent to Ionic Liquid-based solvent ». Licentiate thesis, Luleå tekniska universitet, Energivetenskap, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-84244.
Texte intégralTarkan, Haci Mustafa. « Air-assisted solvent extraction ». Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=102735.
Texte intégralThe novel contribution in this thesis is the production of solvent-coated bubbles by exploiting foaming properties of kerosene-based solvents.
The basic set-up is a chamber to generate foam which is injected through a capillary (orifice diameter 2.5 mm) to produce solvent-coated bubbles (ca. 4.4 mm) which release into the aqueous phase. This generates a solvent specific surface area of ca. 3000 cm-1, equivalent to solvent droplets of ca. 20 mum. Demonstrating the process on dilute Cu solutions (down to 25 mg/L), high aqueous/organic ratios (ca. 75:1) and extractions are achieved. The solvent readily disengages to accumulate at the surface of the aqueous solution.
The LIX family of extractants imparts some foaming to kerosene based solvents but D2EHPA does not. An extensive experimental program determined that 1.5 ppm silicone oil provided the necessary foaming action without affecting extraction or stripping efficiency, greatly expanding the range of solvents that can be used in AASX.
To complement the foam study, films on bubbles blown in solvent were examined by interferometry (film thickness) and infra-red spectroscopy (film composition). A "bound" solvent layer was identified with an initial thickness of ca. 2 - 4 mum, comparable to that determined indirectly (by counting bubbles in an AASX trial and measuring solvent consumption). The film composition appeared to be independent of film thickness as it decreased with time.
As a start to scaling up, the single bubble generation system was adapted by installing up to 8 horizontal capillaries. The bubbles generated were ca. 3.4 mm. Trials showed the multi-bubble set up was a simple replication of the individual bubble case. Preliminary analysis of kinetic data shows a fit to a first-order model.
Brogan, Alex P. S. « Solvent-free liquid proteins ». Thesis, University of Bristol, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.573415.
Texte intégralSackin, Robert. « Solvent ingress in polymers ». Thesis, University of Surrey, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326197.
Texte intégralBajpayee, Anurag. « Directional solvent extraction desalination ». Thesis, Massachusetts Institute of Technology, 2012. http://hdl.handle.net/1721.1/78539.
Texte intégral"September 2012." Cataloged from PDF version of thesis.
Includes bibliographical references (p. 131-137).
World water supply is struggling to meet demand. Production of fresh water from the oceans could supply this demand almost indefinitely. As global energy consumption continues to increase, water and energy resources are getting closely intertwined, especially with regards to the water consumption and contamination in the unconventional oil and gas industry. Development of effective, affordable desalination and water treatment technologies is thus vital to meeting future demand, maintaining economic development, enabling continued growth of energy resources, and preventing regional and international conflict. We have developed a new low temperature, membrane-free desalination technology using directional solvents capable of extracting pure water from a contaminated solution without themselves dissolving in the recovered water. This method dissolves the water into a directional solvent by increasing its temperature, rejects salts and other contaminants, then recovers pure water by cooling back to ambient temperature, and re-uses the solvent. The directional solvents used here include soybean oil, hexanoic acid, decanoic acid, and octanoic acid with the last two observed to be the most effective. These fatty acids exhibit the required characteristics by having a hydrophilic carboxylic acid end which bonds to water molecules but the hydrophobic chain prevents the dissolution of water soluble salts as well the dissolution of the solvent in water. Directional solvent extraction may be considered a molecular-level desalination approach. Directional Solvent Extraction circumvents the need for membranes, uses simple, inexpensive machinery, and by operating at low temperatures offers the potential for using waste heat. This technique also lends itself well to treatment of feed waters over a wide range of total dissolved solids (TDS) levels and is one of the very few known techniques to extract water from saturated brines. We demonstrate >95% salt rejection for seawater TDS concentrations (35,000 ppm) as well as for oilfield produced water TDS concentrations (>100,000 ppm) and saturated brines (300,000 ppm) through a benchtop batch process, and recovery ratios as high as 85% for feed TDS of 35,000 ppm through a multi-stage batch process. We have also designed, constructed, and demonstrated a semi-continuous process prototype. The energy and economic analysis suggests that this technique could become an effective, affordable method for seawater desalination and for treatment of produced water from unconventional oil and gas extraction.
by Anurag Bajpayee.
Ph.D.
TRUJILLO, REBOLLO ANDRES. « SOLVENT EXTRACTION OF MOLYBDENUM ». Diss., The University of Arizona, 1987. http://hdl.handle.net/10150/184009.
Texte intégralLivres sur le sujet "Solvent-solvent"
Chadwick, Oliver, H. Ross Anderson, J. Martin Bland et John Ramsey. Solvent Abuse. New York, NY : Springer New York, 1991. http://dx.doi.org/10.1007/978-1-4612-3184-4.
Texte intégralBarrett, Kevin. Solvent abuse. London : National Society for the Prevention of Cruelty to Children, 1986.
Trouver le texte intégralConnolly, Sean. Solvent abuse. Oxford : Heinemann Library, 2003.
Trouver le texte intégralBirmingham Advisory Committee on Solvent Abuse. Solvent abuse. Birmingham : BACSA, 1987.
Trouver le texte intégralBureau, National Children's, dir. Solvent misuse. London : National Children's Bureau, 1986.
Trouver le texte intégralBirmingham Advisory Committee on Solvent Abuse., dir. Solvent abuse. Birmingham : Birmingham Advisory Committee on Solvent Abuse, 1989.
Trouver le texte intégralArlien-Søborg, Peter. Solvent neurotoxicity. Boca Raton, Fla : CRC Press, 1992.
Trouver le texte intégralUnited States. Environmental Protection Agency. Office of Emergency and Remedial Response. et United States. Environmental Protection Agency. Office of Research and Development., dir. Solvent extraction. Washington, DC : U.S. Environmental Protection Agency, Office of Emergency and Remedial Response, 1994.
Trouver le texte intégralLeahy, R. B. Laboratory comparison of solvent-loaded and solvent-free emulsions. Salem, OR : Oregon Dept. of Transportation, Research Group, 2000.
Trouver le texte intégralCocchiarella, Linda. Stoddard solvent toxicity. Atlanta, GA : U.S. Dept. of Health & Human Services, Public Health Service, Agency for Toxic Substances and Disease Registry, 1993.
Trouver le texte intégralChapitres de livres sur le sujet "Solvent-solvent"
Gooch, Jan W. « Solvent ». Dans Encyclopedic Dictionary of Polymers, 678–82. New York, NY : Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_10886.
Texte intégralLynch, Gordon S., David G. Harrison, Hanjoong Jo, Charles Searles, Philippe Connes, Christopher E. Kline, C. Castagna et al. « Solvent ». Dans Encyclopedia of Exercise Medicine in Health and Disease, 800. Berlin, Heidelberg : Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-540-29807-6_3053.
Texte intégralGooch, Jan W. « Solvent ». Dans Encyclopedic Dictionary of Polymers, 924. New York, NY : Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_14823.
Texte intégralBährle-Rapp, Marina. « solvent ». Dans Springer Lexikon Kosmetik und Körperpflege, 520. Berlin, Heidelberg : Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_9815.
Texte intégralMohamed, Khayet. « Bore Liquid : Solvent and Non-solvent ». Dans Encyclopedia of Membranes, 1–3. Berlin, Heidelberg : Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-40872-4_1180-4.
Texte intégralJones, David T., et David R. Woods. « Solvent Production ». Dans Clostridia, 105–44. Boston, MA : Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-9718-3_4.
Texte intégralMedrzycka, Krystyna, et Sebastian Pastewski. « Solvent Sublation ». Dans Chemistry for the Protection of the Environment 2, 67–74. Boston, MA : Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0405-0_8.
Texte intégralMorgan, Michael M., MacDonald J. Christie, Luis De Lecea, Jason C. G. Halford, Josee E. Leysen, Warren H. Meck, Catalin V. Buhusi et al. « Solvent Abuse ». Dans Encyclopedia of Psychopharmacology, 1252. Berlin, Heidelberg : Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_3587.
Texte intégralGooch, Jan W. « Adhesive, Solvent ». Dans Encyclopedic Dictionary of Polymers, 20. New York, NY : Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_276.
Texte intégralGooch, Jan W. « Differentiating Solvent ». Dans Encyclopedic Dictionary of Polymers, 219. New York, NY : Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_3649.
Texte intégralActes de conférences sur le sujet "Solvent-solvent"
Gupta, Subodh Chandra, Simon Gittins, Arun Sood et Khalil Zeidani. « Optimal Amount of Solvent in Solvent Aided Process ». Dans Canadian Unconventional Resources and International Petroleum Conference. Society of Petroleum Engineers, 2010. http://dx.doi.org/10.2118/137543-ms.
Texte intégralGupta, Subodh Chandra, et Simon Gittins. « Measurement of Recovered Solvent in Solvent Aided Process ». Dans Canadian Unconventional Resources and International Petroleum Conference. Society of Petroleum Engineers, 2010. http://dx.doi.org/10.2118/136402-ms.
Texte intégralIvory, J., T. Frauenfeld et C. Jossy. « Thermal Solvent Reflux and Thermal Solvent Hybrid Experiments ». Dans Canadian International Petroleum Conference. Petroleum Society of Canada, 2007. http://dx.doi.org/10.2118/2007-067.
Texte intégralChang, Jeannine, John Joseph Ivory, Ken Forshner et Yu Feng. « Impact Of Solvent Loss During Solvent Injection Processes ». Dans SPE Heavy Oil Conference-Canada. Society of Petroleum Engineers, 2013. http://dx.doi.org/10.2118/165476-ms.
Texte intégralRasaiah, Jayendran C., et Jianjun Zhu. « Solvent dynamics and electron transfer reactions ». Dans Ultrafast reaction dynamics and solvent effects. AIP, 1994. http://dx.doi.org/10.1063/1.45397.
Texte intégralMialocq, J. C., P. Hébert, G. Baldacchino et T. Gustavsson. « Relaxation dynamics of a polar solvent cage around a nonpolar electronically excited solvent probe. A subpicosecond laser study ». Dans Ultrafast reaction dynamics and solvent effects. AIP, 1994. http://dx.doi.org/10.1063/1.45390.
Texte intégralBalos, Vasileios, Hossam Elgabarty, Martin Wolf, Thomas Kühne, Roland Netz, Douwe Jan Bonthuis, Naveen Kumar Kaliannan, Philip Loche, Tobias Kampfrath et Mohsen Sajadi. « Ultrafast solvent-to-solvent and solvent-to-solute energy transfer driven by single-cycle THz electric fields ». Dans Terahertz Emitters, Receivers, and Applications XII, sous la direction de Manijeh Razeghi et Alexei N. Baranov. SPIE, 2021. http://dx.doi.org/10.1117/12.2594143.
Texte intégralMuguet, Francis F., et G. Wilse Robinson. « Energetics and formation of the ‘‘hydrated electron’’ within an itinerant radical model ». Dans Ultrafast reaction dynamics and solvent effects. AIP, 1994. http://dx.doi.org/10.1063/1.45404.
Texte intégralGrabowska, A. « Proton transfer reactions prepared by the hydrogen bonds in electronically excited polyatomic molecules ». Dans Ultrafast reaction dynamics and solvent effects. AIP, 1994. http://dx.doi.org/10.1063/1.45385.
Texte intégralDeclémy, Alain, et Claude Rullière. « Relaxation dynamics of the solvent cage around an excited molecule in solution ». Dans Ultrafast reaction dynamics and solvent effects. AIP, 1994. http://dx.doi.org/10.1063/1.45386.
Texte intégralRapports d'organisations sur le sujet "Solvent-solvent"
Klatt, L. N. Caustic-Side Solvent Extraction Solvent-Composition Recommendation. Office of Scientific and Technical Information (OSTI), mai 2002. http://dx.doi.org/10.2172/814130.
Texte intégralFraga, Carlos, Kai-For Mo, David Abrecht, Amanda Casella, Nicolas Uhnak, Zachary Kennedy et Gregg Lumetta. Solvent Exchange. Office of Scientific and Technical Information (OSTI), septembre 2020. http://dx.doi.org/10.2172/1983975.
Texte intégralLeonard, R. A. Caustic-side solvent extraction Flowsheet for optimized solvent. Office of Scientific and Technical Information (OSTI), juillet 2002. http://dx.doi.org/10.2172/799858.
Texte intégralDelmau, Laetitia Helene, et Bruce A. Moyer. Solvent Blending Strategy to Upgrade MCU CSSX Solvent to Equivalent Next-Generation CSSX Solvent. Office of Scientific and Technical Information (OSTI), décembre 2012. http://dx.doi.org/10.2172/1057946.
Texte intégralMoyer, Bruce, et Nathan Bessen. Density of Next-Generation Caustic-Side Solvent Extraction Solvent. Office of Scientific and Technical Information (OSTI), août 2021. http://dx.doi.org/10.2172/1819565.
Texte intégralPaffhausen, M. W., D. L. Smith et S. N. Ugaki. Solvent recycle/recovery. Office of Scientific and Technical Information (OSTI), septembre 1990. http://dx.doi.org/10.2172/6153281.
Texte intégralCrowder, M. L. Solvent Quality Testing. Office of Scientific and Technical Information (OSTI), septembre 2002. http://dx.doi.org/10.2172/802626.
Texte intégralLeigh R. Martin et Bruce J. Mincher. TALSPEAK Solvent Degradation. Office of Scientific and Technical Information (OSTI), septembre 2009. http://dx.doi.org/10.2172/971366.
Texte intégralBonnesen, P. V. Stability of the Caustic-Side Solvent Extraction (CSSX) Process Solvent : Effect of High Nitrite on Solvent Nitration. Office of Scientific and Technical Information (OSTI), juin 2002. http://dx.doi.org/10.2172/814158.
Texte intégralDuncan, Nathan C., Laetitia Helene Delmau, Dale Ensor, Denise L. Lee, Joseph F. Birdwell Jr, Talon G. Hill, Neil J. Williams et al. Next Generation Solvent Development for Caustic-Side Solvent Extraction of Cesium. Office of Scientific and Technical Information (OSTI), juillet 2013. http://dx.doi.org/10.2172/1087500.
Texte intégral