Thèses sur le sujet « SOLVENT SYSTEMS »
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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.
Texte intégralCheng, Chin-Hwa 1957. « Solubility of diuron in complex solvent systems ». Thesis, The University of Arizona, 1989. http://hdl.handle.net/10150/277194.
Texte intégralLunkov, Sergey. « Modelling metal complexation in solvent extraction systems ». Thesis, Curtin University, 2013. http://hdl.handle.net/20.500.11937/2018.
Texte intégralBrindle, David. « Lattice models of amphiphile and solvent mixtures ». Thesis, Sheffield Hallam University, 1991. http://shura.shu.ac.uk/19397/.
Texte intégralLesutis, Heather Patrick. « Reaction kinetics in environmentally benign novel solvent systems ». Diss., Georgia Institute of Technology, 2000. http://hdl.handle.net/1853/11865.
Texte intégralBailie, David S. « Homogeneous oxidation catalysis in multiphasic liquid solvent systems ». Thesis, Queen's University Belfast, 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.675950.
Texte intégralPayne, Kathryn Elizabeth Ann. « Pigment-dispersant-solvent interactions appropriate to paint systems ». Thesis, London South Bank University, 1998. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.267389.
Texte intégralHealy, Mary Rose. « Outer-sphere interactions in metal solvent extraction systems ». Thesis, University of Edinburgh, 2017. http://hdl.handle.net/1842/28712.
Texte intégralCocchi, Giovanni <1984>. « Thermodynamic and mechanical properties of polymer-solvent systems ». Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2013. http://amsdottorato.unibo.it/5782/1/cocchi_giovanni_tesi.pdf.
Texte intégralQuesto lavoro verte sulla caratterizzazione teorica e sperimentale delle proprietà termodinamiche, meccaniche e di trasporto di sistemi polimero-solvente. In particolare sono stati presi in considerazione sia sistemi polimero-solvente in cui la matrice polimerica si trova allo stato di gomma, che sistemi in cui la matrice polimerica esibisce comportamento vetroso, nonché sistemi nei quali si verifica la transizione vetrosa indotta dall'effetto plasticizzante del solvente. La modellazione termodinamica è stata effettuata utilizzando equazioni di stato avanzate e metodi idonei ad estenderne il campo di utilizzo alla condizione di non equilibrio, propria dello stato vetroso. Cinetiche di assorbimento non Fickiane sono state modellate utilizzando approcci fenomenologici e modelli cinetici avanzati.
Cocchi, Giovanni <1984>. « Thermodynamic and mechanical properties of polymer-solvent systems ». Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2013. http://amsdottorato.unibo.it/5782/.
Texte intégralQuesto lavoro verte sulla caratterizzazione teorica e sperimentale delle proprietà termodinamiche, meccaniche e di trasporto di sistemi polimero-solvente. In particolare sono stati presi in considerazione sia sistemi polimero-solvente in cui la matrice polimerica si trova allo stato di gomma, che sistemi in cui la matrice polimerica esibisce comportamento vetroso, nonché sistemi nei quali si verifica la transizione vetrosa indotta dall'effetto plasticizzante del solvente. La modellazione termodinamica è stata effettuata utilizzando equazioni di stato avanzate e metodi idonei ad estenderne il campo di utilizzo alla condizione di non equilibrio, propria dello stato vetroso. Cinetiche di assorbimento non Fickiane sono state modellate utilizzando approcci fenomenologici e modelli cinetici avanzati.
Draucker, Laura Christine. « Novel Solvent Systems for the Development of Sustainable Technology ». Diss., Georgia Institute of Technology, 2007. http://hdl.handle.net/1853/16188.
Texte intégralBelhadj, Hamza [Verfasser]. « Solvent isotope effect (D2O) in photocatalytic systems / Hamza Belhadj ». Hannover : Technische Informationsbibliothek (TIB), 2017. http://d-nb.info/1150536683/34.
Texte intégralChen, Zhihong. « Morphology of, and solvent diffusion in, hollow nanoparticle systems ». Thesis, University of Sheffield, 2014. http://etheses.whiterose.ac.uk/5019/.
Texte intégralDreimann, Jens M. [Verfasser]. « Process Intensification in Homogeneous Catalysis - Catalyst Recovery via Thermomorphic Solvent Systems and Organic Solvent Nanofiltration / Jens M. Dreimann ». München : Verlag Dr. Hut, 2017. http://d-nb.info/1139538349/34.
Texte intégralDreimann, Jens [Verfasser]. « Process Intensification in Homogeneous Catalysis - Catalyst Recovery via Thermomorphic Solvent Systems and Organic Solvent Nanofiltration / Jens M. Dreimann ». München : Verlag Dr. Hut, 2017. http://d-nb.info/1139538349/34.
Texte intégralHamilton, Patrick Neal. « The behavior and separation of polystyrene in mixed solvent systems ». [College Station, Tex. : Texas A&M University, 2007. http://hdl.handle.net/1969.1/ETD-TAMU-1256.
Texte intégralBaranowski, Roman. « The properties of polymer/solvent systems at surfaces and interfaces ». Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/nq25767.pdf.
Texte intégralPitt, Julian Llewellyn. « The behaviour of mineral particles in uranium solvent extraction systems ». Thesis, Imperial College London, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.339619.
Texte intégralRivett, Carl Matthew. « Carbon Dioxide as a Solvent and Antisolvent for Hydrocarbon Systems ». Thesis, University of East Anglia, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.518387.
Texte intégralHelal, Hatem Hamdi Ahmed. « Including solvent effects in first-principles simulations of biological systems : development, implementation, and application of an implicit solvent model ». Thesis, University of Cambridge, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.609182.
Texte intégralHusain, Zainul Abideen. « Coupling reactions and separations in propane-organic-aqueous tunable solvent systems ». Thesis, Atlanta, Ga. : Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/29719.
Texte intégralCommittee Chair: Eckert, Charles; Committee Co-Chair: Liotta, Charles; Committee Member: Meredith, Carson. Part of the SMARTech Electronic Thesis and Dissertation Collection.
Hafner, Kellye Padgett. « Design of solvent systems for supercritical fluid and high pressure applications ». Diss., Georgia Institute of Technology, 1996. http://hdl.handle.net/1853/11211.
Texte intégralTheaker, 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.
Texte intégralChavez, Krystle J. « Crystallization of pseudopolymorphic forms of sodium naproxen in mixed solvent systems ». Diss., Atlanta, Ga. : Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/29759.
Texte intégralCommittee Chair: Rousseau, Ronald; Committee Member: Meredith, Carson; Committee Member: Prausnitz, Mark; Committee Member: Teja, Amyn; Committee Member: Wilkinson, Angus. Part of the SMARTech Electronic Thesis and Dissertation Collection.
Das, Mousumi. « Physico-chemical investigation of transport and thermodynamic properties of some electrolytes in verious solvent systems ». Thesis, University of North Bengal, 2007. http://hdl.handle.net/123456789/817.
Texte intégralEckert, Norbert L. « Aspects of phase separation in an experimental mixer-settler using two solvent extraction systems ». Thesis, University of British Columbia, 1987. http://hdl.handle.net/2429/26697.
Texte intégralApplied Science, Faculty of
Chemical and Biological Engineering, Department of
Graduate
Rieck, Daniel C. « MEMS fabricated nanopores and micropores functionalized with chromate-selective solvent polymeric membrane ». Pullman, Wash. : Washington State University, 2008. http://www.dissertations.wsu.edu/Thesis/Fall2008/d_rieck_012609.pdf.
Texte intégralTitle from PDF title page (viewed on Apr. 10, 2009). "Department of Chemical Engineering." Includes bibliographical references.
Cecconie, Theodore James 1961. « Fundamental studies on the separation of the lanthanides using solvent extraction systems ». Thesis, The University of Arizona, 1988. http://hdl.handle.net/10150/276744.
Texte intégralMuhuri, Prakash Kumar. « Studies on the ion-solvent interactions of some electrolytes in propylene carbonate and its binary mixtures with other organic solvent systems ». Thesis, University of North Bengal, 1993. http://hdl.handle.net/123456789/710.
Texte intégralSinha, Anuradha. « Investigation on viscous synergy and antagonism of some liquid mixtures and ion-solvent interaction of some compounds in various solvent systems ». Thesis, University of North Bengal, 2006. http://hdl.handle.net/123456789/705.
Texte intégralBrunet, Jean-Christophe. « An expert system for solvent-based separation process synthesis ». Thesis, Virginia Tech, 1992. http://hdl.handle.net/10919/42949.
Texte intégralMaster of Science
Horne, Gregory. « An experimental and computational investigation into the radiolysis of PUREX solvent systems ». Thesis, University of Manchester, 2016. https://www.research.manchester.ac.uk/portal/en/theses/an-experimental-and-computational-investigation-into-the-radiolysis-of-purex-solvent-systems(a793f6ee-0b49-47ce-ae2b-cd88d94c53a0).html.
Texte intégralTian, Olivia Yingnan. « Pigmented and solvent dyed latex systems for ink jet printing on textiles ». Thesis, Georgia Institute of Technology, 1998. http://hdl.handle.net/1853/8681.
Texte intégralNzengung, Valentine Asongu. « Organoclays as sorbents for organic contaminants in aqueous and mixed-solvent systems ». Diss., Georgia Institute of Technology, 1993. http://hdl.handle.net/1853/26460.
Texte intégralMcGillen, J. G. « Studies on the wet spinning of cellulose fibres from novel solvent systems ». Thesis, University of Strathclyde, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.372448.
Texte intégralGumus, Selahaddin. « Secondary Electronic and Solvent Effects on Regiospecific P-Bromination of Aromatic Systems ». TopSCHOLAR®, 2018. https://digitalcommons.wku.edu/theses/3031.
Texte intégralAPRAHAMIAN, EDWARD JR. « ROLE OF THE INTERFACE IN THE KINETICS AND MECHANISM OF SOLVENT EXTRACTION SYSTEMS (DITHIZONE, OXINE, INTERFACIAL AREA, DISPERSION) ». Diss., The University of Arizona, 1985. http://hdl.handle.net/10150/187968.
Texte intégralKhalid, Muhammad. « Influence of solvent viscosity, polarity and polarizability on the chemiluminescence parameters of inter and intramolecular electron transfer initiated chemiexcitation systems ». Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-29092015-114251/.
Texte intégralOs peróxidos cíclicos: peróxido de difenoila (1), spiro-adamantil-1,2-dioxetanona (2) e 4-(3-terc-butildimetilsililoxifenil)-4-metoxispiro[1,2-dioxetano-3.2\'-adamantano] (3) foram sintetizados, purificados e caracterizados e as suas propriedades cinéticas e de quimiluminescência (CL) determinadas. A influência da polaridade do solvente sobre os parâmetros de quimi-excitação da decomposição catalisada de 1 e 2, e a decomposição induzida de 3 foi examinada em diversas misturas binárias de solventes com parâmetros de polaridade e polarizabilidade diferente, mas viscosidades semelhantes. Para solventes com baixa polaridade, os rendimentos quânticos singlete para a decomposição catalisada intermolecular do peróxido de difenoila (1) e 1,2-dioxetanona (2) aumentam em função da polaridade do meio, mostrando valores máximos em meios com polaridade intermediária, e diminuim para misturas altamente polares. Para a decomposição induzida de 3, o rendimento quântico mostrou aumentar com o aumento da polaridade do solvente, inclusive para sistemas com alta polaridade. Nos sistemas binários de solventes estudados, os parâmetros de polarizabilidade mostraram-se contrários aos valores de polaridade, portanto, parece que um aumento da polarizability leva a uma diminuição nos rendimentos quânticos singlete para a decomposição catalisada do peróxido de difenoila (1) e a decomposição induzida de 3, no entanto, um aumento nos rendimentos quânticos singlete para a 1,2-dioxetanona 2. Os três sistemas de CL também foram estudados em misturas binárias de solventes com diferentes viscosidades, mas com parâmetros de polaridade e polarizabilidade semelhantes e os rendimentos quânticos singlete mostraram aumentar com o aumento da viscosidade do meio. Os dados foram analisados usando tanto o modelos colisional quando o modelo de volume livre. Surpreendentemente, o sistema altamente eficiente decomposição induzida intramolecular do 1,2-dioxetano 3 mostrou-se muito mais sensível aos efeitos da viscosidade do que os sistemas intermoleculares ineficientes, o que indica claramente que a decomposição induzida do 1,2-dioxetano deve ocorrer por um processo de retro-transferência de elétron intramolecular. Além disso, os parâmetros de quimiluminescência destes sistemas foram estudados em vários solventes puros. Os rendimentos quânticos singlete obtidos foram correlacionados com parâmetros de viscosidade, polarizabilidade e polaridade usando análise de regressão linear múltipla.
Cikalo, Maria Gillian. « Separation and quantification of weakly-absorbing and low-concentration analytes by capillary electrophoresis ». Thesis, University of York, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.321675.
Texte intégralDatta, Biswajit. « Exploration of miscellaneous interfaces of some ionic solids and ionic liquids Prevailing in various solvent systems by the process of psysicochemical contrivance ». Thesis, University of North Bengal, 2017. http://ir.nbu.ac.in/handle/123456789/2673.
Texte intégralChunsrivirot, Surasak. « Binding affinity of a small molecule to an amorphous polymer in a solvent ». Thesis, Massachusetts Institute of Technology, 2011. http://hdl.handle.net/1721.1/65771.
Texte intégralPage 169 blank. Cataloged from PDF version of thesis.
Includes bibliographical references (p. 165-168).
Crystallization is a commonly used purification process in industrial practice. It usually begins with heterogeneous nucleation on a foreign surface. The complicated mechanism of heterogeneous nucleation is not well understood, but we hypothesize a possible correlation between binding affinity to a surface and nucleation enhancement. Amorphous polymers have been used in controlling crystallization. However, to our knowledge no attempt has been made to investigate the possibility of using binding affinity to help guide the selection of polymers promoting heterogeneous nucleation. This study investigated the possibility of using binding affinity of one molecule and many molecules to help guide the selection of these polymers. To measure the binding affinity of one molecule, we developed a two-step approach to compute the free energy of binding to a binding site, using a system of ethylene glycol, polyvinyl alcohol (PVA), and heavy water (D20). The first step of our approach uses Adsorption Locator to identify probable binding sites and molecular dynamics to screen for the best binding sites. The second step employs the Blue-Moon Ensemble method to compute the free energy of binding. We then applied our procedure to the systems of aspirin binding on the surfaces of four nonporous crosslinked polymers in ethanol-water 38 v%. These polymers are poly(4- acryloylmorpholine) (PAM), poly(2-carboxyethyl acrylate) (PCEA), poly(4-hydroxylbutyl acrylate) (PHBA), and polystyrene (PS), and they all are crosslinked with divinylbenzene (DVB). We developed an approach to construct these crosslinked polymers and built three independent surfaces for each polymer. We found the similarity between the trend of heterogeneous nucleation activity and that of the average free energies of binding to the best site of each polymer surface. To measure the binding affinity of many molecules, preferential interaction coefficient and the number of aspirin molecules associated with the area of the binding site was calculated. We found that there is also a similarity between the trend of heterogeneous nucleation activity and that of number of aspirin molecules associated with the area of the binding site (taken into account the effects of polar/apolar atom interactions between an aspirin and a polymer). These results suggest the possibility of using binding affinity, especially the free energy of binding to the best site and the number of nucleating molecule, to help guide the selection of polymers promoting heterogeneous nucleation.
by Surasak Chunsrivirot.
Ph.D.
Julien, Grégoire. « Dynamics in polymer blends and polymer-solvent blends close to the glass transition ». Thesis, Lyon 1, 2014. http://www.theses.fr/2014LYO10187/document.
Texte intégralIn this work, we propose a model for describing the dynamics in polymer blends or polymer-solvent blends close to and below Tg. The model is solved on a 2D lattice corresponding to spatial scales from 10 nm up to a few micrometers and incorporate the heterogeneous nature of the dynamics at the scale of a dynamic heterogeneity (3-5 nm). In case of polymer blends, we apply this model to study phase separation close to and below Tg upon cooling, and rejuvenation in miscible range upon heating. In the course of phase separation, we observe slow structures forming in coexistence with faster ones. In the same time, the global dynamics of the system slows down and domains grow like the logarithm of the time. During rejuvenation, we observe that morphologies melt much faster the elapsed time required to build them during aging. In the case of polymer-solvent blends, the system is put in contact with a solvent reservoir and is at temperatures far below the pure polymer glass transition. We consider situations where the activity of the solvent reservoir is varied in order to describe either films drying or swelling. Our model allows for explaining case-II diffusion in the context of the plasticisation of a glassy polymer by penetrating solvent during swelling. Regarding the process of film drying, we show that films up to 1 micrometer thick can be completely dried. When drying a thicker film, we show that a glassy crust may appear on the free surface, as shown experimentally
Das, Bijan. « Physico - chemical investigations on the ion-solvent interactions of some Tetraalkylammonium and common ions in non-aqueous and mixed binary aqueous solvent systems ». Thesis, University of North Bengal, 1992. http://hdl.handle.net/123456789/719.
Texte intégralAdinata, Donni [Verfasser]. « Single-drop based modelling of solvent extraction in high-viscosity systems / Donni Adinata ». Aachen : Hochschulbibliothek der Rheinisch-Westfälischen Technischen Hochschule Aachen, 2011. http://d-nb.info/1018200606/34.
Texte intégralChang, Yun Chea. « Concentration dependent diffusion of solid-solute, liquid-solvent systems in the supersautrated region ». Diss., Georgia Institute of Technology, 1985. http://hdl.handle.net/1853/11802.
Texte intégralGautam, Devaki Nandan. « Molecular dynamics simulation of horse-heart cytochrome c in water-methanol solvent systems ». Thesis, Wichita State University, 2014. http://hdl.handle.net/10057/10956.
Texte intégralThesis (M.S.)--Wichita State University, Fairmount College of Liberal Arts, Dept. of Chemistry
Van, Deventer David. « Discrimination of Retained Solvent Levels in Printed Food-Packaging Using Electronic Nose Systems ». Thesis, Virginia Tech, 2000. http://hdl.handle.net/10919/9741.
Texte intégralMaster of Science
Lin, Tingdong. « On the phase behavior and particle formation in polyimide/solvent/nonsolvent ternary systems ». Diss., This resource online, 1993. http://scholar.lib.vt.edu/theses/available/etd-06062008-165916/.
Texte intégralEser, Hülya Tıhmınlıoğlu Funda. « Diffusion And Equilibrium Measurements In Polymer-Solvent Systems By Inverse Gas Chromatography Method/ ». [s.l.] : [s.n.], 2004. http://library.iyte.edu.tr/tezler/master/kimya/T000451.pdf.
Texte intégralKobayashi, Takashi. « Development of Reactor Systems Based on Kinetic Analysis of β-Glucosidase-or Lipase-catalyzed Condensation in Organic Solvent Systems ». Kyoto University, 2003. http://hdl.handle.net/2433/148961.
Texte intégral0048
新制・課程博士
博士(農学)
甲第10232号
農博第1304号
新制||農||862(附属図書館)
学位論文||H15||N3753(農学部図書室)
UT51-2003-H653
京都大学大学院農学研究科応用生命科学専攻
(主査)教授 松野 隆一, 教授 大東 肇, 教授 井上 國世
学位規則第4条第1項該当