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Artykuły w czasopismach na temat "Ionic strength"
Kreusser, Jannette, Fabian Jirasek i Hans Hasse. "Influence of Salts on the Adsorption of Lysozyme on a Mixed-Mode Resin". Adsorption Science & Technology 2021 (23.01.2021): 1–11. http://dx.doi.org/10.1155/2021/6681348.
Pełny tekst źródłaPham, T. V., i K. C. Westaway. "Solvent effects on nucleophilic substitution reactions. III. The effect of adding an inert salt on the structure of the SN2 transition state". Canadian Journal of Chemistry 74, nr 12 (1.12.1996): 2528–30. http://dx.doi.org/10.1139/v96-283.
Pełny tekst źródłaDolling, PJ, i GSP Ritchie. "Estimates of soil solution ionic strength and the determination of pH in West Australian soils". Soil Research 23, nr 2 (1985): 309. http://dx.doi.org/10.1071/sr9850309.
Pełny tekst źródłaAltamash, Tausif, Wesam Ahmed, Saad Rasool i Kabir H. Biswas. "Intracellular Ionic Strength Sensing Using NanoLuc". International Journal of Molecular Sciences 22, nr 2 (12.01.2021): 677. http://dx.doi.org/10.3390/ijms22020677.
Pełny tekst źródłaDickhout, Janneke, Rob Lammertink i Wiebe de Vos. "Membrane Filtration of Anionic Surfactant Stabilized Emulsions: Effect of Ionic Strength on Fouling and Droplet Adhesion". Colloids and Interfaces 3, nr 1 (10.01.2019): 9. http://dx.doi.org/10.3390/colloids3010009.
Pełny tekst źródłaBorah, Priyanka, i Venkata S. K. Mattaparthi. "Effect of Ionic Strength on the Aggregation Propensity of Aβ1-42 Peptide: An In-silico Study". Current Chemical Biology 14, nr 3 (28.12.2020): 216–26. http://dx.doi.org/10.2174/2212796814999200818103157.
Pełny tekst źródłaKosmulski, Marek, i Jarl B. Rosenholm. "High ionic strength electrokinetics". Advances in Colloid and Interface Science 112, nr 1-3 (grudzień 2004): 93–107. http://dx.doi.org/10.1016/j.cis.2004.09.005.
Pełny tekst źródłaBucko, Sandra, Jaroslav Katona, Ljiljana Popovic, Zuzana Vastag i Lidija Petrovic. "Functional properties of pumpkin (Cucurbita pepo) seed protein isolate and hydrolysate". Journal of the Serbian Chemical Society 81, nr 1 (2016): 35–46. http://dx.doi.org/10.2298/jsc150615081b.
Pełny tekst źródłaManono, Malibongwe, Kirsten Corin i Jenny Wiese. "The Effect of the Ionic Strength of Process Water on the Interaction of Talc and CMC: Implications of Recirculated Water on Floatable Gangue Depression". Minerals 9, nr 4 (15.04.2019): 231. http://dx.doi.org/10.3390/min9040231.
Pełny tekst źródłaSundman, Ola, Per Persson i Lars-Olof Öhman. "Comparison between specific surface complexation and Donnan ion-exchange models for describing the adsorption of cations on kraft fibres – literature evidence and EXAFS study of Cu(II) binding". Nordic Pulp & Paper Research Journal 25, nr 2 (1.05.2010): 178–84. http://dx.doi.org/10.3183/npprj-2010-25-02-p178-184.
Pełny tekst źródłaRozprawy doktorskie na temat "Ionic strength"
Beriet, Carine. "Microelectrode studies in low ionic strength media". Thesis, University of Southampton, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.241602.
Pełny tekst źródłaBlair, Laura May. "Optimizing growth in low ionic strength solutions and the ameliorative effects of increased ionic strength on copper toxicity in Triticum aestivum (wheat) /". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp04/mq22574.pdf.
Pełny tekst źródłaWeidgans, Bernhard M. "New fluorescent optical pH sensors with minimal effects of ionic strength". [S.l.] : [s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=97274679X.
Pełny tekst źródłaMarcera, Donna M. "Conformational studies of carboxymethylcellulose in aqueous saline solutions as a function of ionic strength /". Online version of thesis, 1990. http://hdl.handle.net/1850/10684.
Pełny tekst źródłaDeeyaa, Blessing D. "DNA Photocleavage by 9-Aminomethylanthracene Dyes at pH 7.0: Ionic Strength Effects". Digital Archive @ GSU, 2011. http://digitalarchive.gsu.edu/chemistry_theses/39.
Pełny tekst źródłaHe, Yongtian. "Chromate reduction and immobilization under high pH and high ionic strength conditions". Columbus, OH : Ohio State University, 2003. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1047476794.
Pełny tekst źródłaTitle from first page of PDF file. Document formatted into pages; contains xix, 219 p.: ill. (some col.). Includes abstract and vita. Advisor: Samuel J. Traina, Environmental Science Graduate Program. Includes bibliographical references (p. 201-219).
Carvajal-Figueroa, Maria Teresa 1959. "Solubility of quinoline in aqueous systems: Effect of pH and ionic strength". Thesis, The University of Arizona, 1989. http://hdl.handle.net/10150/291584.
Pełny tekst źródłaPatterson, Adele. "Retention properties of porous graphite". Thesis, University of Nottingham, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.342124.
Pełny tekst źródłaHossain, Mohammad Moshin. "Effects of HCO3- and ionic strength on the oxidation and dissolution of UO2". Licentiate thesis, KTH, Chemistry, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4172.
Pełny tekst źródłaThe kinetics for radiation induced dissolution of spent nuclear fuel is a key issue in the safety assessment of a future deep repository. Spent nuclear fuel mainly consists of UO2 and therefore the release of radionuclides (fission products and actinides) is assumed to be governed by the oxidation and subsequent dissolution of the UO2 matrix. The process is influenced by the dose rate in the surrounding groundwater (a function of fuel age and burn up) and on the groundwater composition. In this licentiate thesis the effects of HCO3- (a strong complexing agent for UO22+) and ionic strength on the kinetics of UO2 oxidation and dissolution of oxidized UO2 have been studied experimentally.
The experiments were performed using aqueous UO2 particle suspensions where the oxidant concentration was monitored as a function of reaction time. These reaction systems frequently display first order kinetics. Second order rate constants were obtained by varying the solid UO2 surface area to solution volume ratio and plotting the resulting pseudo first order rate constants against the surface area to solution volume ratio. The oxidants used were H2O2 (the most important oxidant under deep repository conditions), MnO4- and IrCl62-. The kinetics was studied as a function of HCO3- concentration and ionic strength (using NaCl and Na2SO4 as electrolytes).
The rate constant for the reaction between H2O2 and UO2 was found to increase linearly with the HCO3- concentration in the range 0-1 mM. Above 1 mM the rate constant is independent of the HCO3- concentration. The HCO3- concentration independent rate constant is interpreted as being the true rate constant for oxidation of UO2 by H2O2 [(4.4 ± 0.3) x 10-6 m min-1] while the HCO3- concentration dependent rate constant is used to estimate the rate constant for HCO3- facilitated dissolution of UO22+ (oxidized UO2) [(8.8 ± 0.5) x 10-3 m min-1]. From experiments performed in suspensions free from HCO3- the rate constant for dissolution of UO22+ was also determined [(7 ± 1) x 10-8 mol m-2 s-1]. These rate constants are of significant importance for simulation of spent nuclear fuel dissolution.
The rate constant for the oxidation of UO2 by H2O2 (the HCO3- concentration independent rate constant) was found to be independent of ionic strength. However, the rate constant for dissolution of oxidized UO2 displayed ionic strength dependence, namely it increases with increasing ionic strength.
The HCO3- concentration and ionic strength dependence for the anionic oxidants is more complex since also the electron transfer process is expected to be ionic strength dependent. Furthermore, the kinetics for the anionic oxidants is more pH sensitive. For both MnO4- and IrCl62- the rate constant for the reaction with UO2 was found to be diffusion controlled at higher HCO3- concentrations (~0.2 M). Both oxidants also displayed ionic strength dependence even though the HCO3- independent reaction could not be studied exclusively.
Based on changes in reaction order from first to zeroth order kinetics (which occurs when the UO2 surface is completely oxidized) in HCO3- deficient systems the oxidation site density of the UO2 powder was determined. H2O2 and IrCl62- were used in these experiments giving similar results [(2.1 ± 0.1) x 10-4 and (2.7 ± 0.5) x 10-4 mol m-2, respectively].
Hossain, Mohammad Moshin. "Effects of HCO₃- and ionic strength on the oxidation and dissolution of UO₂ /". Stockholm : Chemical Science and Engineering, KTH, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4172.
Pełny tekst źródłaKsiążki na temat "Ionic strength"
Reed, Donald T., Sue B. Clark i Linfeng Rao, red. Actinide Speciation in High Ionic Strength Media. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4419-8690-0.
Pełny tekst źródłaJohnsson, Patricia A. A computer program for geochemical analysis of acid-rain and other low-ionic-strength, acidic waters. West Trenton, N.J: Dept. of the Interior, U.S. Geological Survey, 1987.
Znajdź pełny tekst źródłaTurner, J. D. Development of an optical pH sensor for the range 7-10pH units suitable for low ionic strength solutions. Manchester: UMIST, 1995.
Znajdź pełny tekst źródłaW, Farrar Jerry, i Geological Survey (U.S.), red. Report on the U.S. Geological Survey's evaluation program for standard reference samples distributed in October 1992, T-121 (trace constituents), M-124 (major constituents), N-36 (nutrients), N-37 (nutrients), P-19 (low ionic strength) and Hg-15 (mercury). Golden, Colo: Dept. of the Interior, U.S. Geological Survey, 1993.
Znajdź pełny tekst źródłaW, Farrar Jerry, i Geological Survey (U.S.), red. Report on the U.S. Geological Survey's evaluation program for standard reference samples distributed in October 1992, T-121 (trace constituents), M-124 (major constituents), N-36 (nutrients), N-37 (nutrients), P-19 (low ionic strength) and Hg-15 (mercury). Golden, Colo: Dept. of the Interior, U.S. Geological Survey, 1993.
Znajdź pełny tekst źródłaW, Farrar Jerry, i Geological Survey (U.S.), red. Report on the U.S. Geological Survey's evaluation program for standard reference samples distributed in October 1992, T-121 (trace constituents), M-124 (major constituents), N-36 (nutrients), N-37 (nutrients), P-19 (low ionic strength) and Hg-15 (mercury). Golden, Colo: Dept. of the Interior, U.S. Geological Survey, 1993.
Znajdź pełny tekst źródłaW, Farrar Jerry, i Geological Survey (U.S.), red. Report on the U.S. Geological Survey's evaluation program for standard reference samples distributed in October 1992, T-121 (trace constituents), M-124 (major constituents), N-36 (nutrients), N-37 (nutrients), P-19 (low ionic strength) and Hg-15 (mercury). Golden, Colo: Dept. of the Interior, U.S. Geological Survey, 1993.
Znajdź pełny tekst źródłaW, Farrar Jerry, i Geological Survey (U.S.), red. Report on the U.S. Geological Survey's evaluation program for standard reference samples distributed in October 1992, T-121 (trace constituents), M-124 (major constituents), N-36 (nutrients), N-37 (nutrients), P-19 (low ionic strength) and Hg-15 (mercury). Golden, Colo: Dept. of the Interior, U.S. Geological Survey, 1993.
Znajdź pełny tekst źródłaW, Farrar Jerry, i Geological Survey (U.S.), red. Report on the U.S. Geological Survey's evaluation program for standard reference samples distributed in October 1994: T-131 (trace constituents), T-133 (trace constituents), M-132 (major constituents), N-43 (nutrients), N-44 (nutrients), P-23 (low ionic strength) and Hg-19 (mercury). Golden, Colo: Dept. of the Interior, U.S. Geological Survey, 1995.
Znajdź pełny tekst źródłaW, Farrar Jerry, i Geological Survey (U.S.), red. Report on the U.S. Geological Survey's evaluation program for standard reference samples distributed in May 1995: T-135 (trace constituents), M-134 (major constituents), N-45 (nutrients), N-46 (nutrients), P-24 (low ionic strength), Hg-20 (mercury), and SED-5 (bed material). Golden, Colo: U.S. Dept. of the Interior, U.S. Geological Survey, 1995.
Znajdź pełny tekst źródłaCzęści książek na temat "Ionic strength"
Gooch, Jan W. "Ionic Strength". W Encyclopedic Dictionary of Polymers, 902. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_14051.
Pełny tekst źródłaPardue, Harry L. "Effects of Ionic Strength". W Chemical Equilibria, 1–16. Boca Raton: CRC Press, Taylor & Francis Group, 2019.: CRC Press, 2018. http://dx.doi.org/10.1201/9780429429897-1.
Pełny tekst źródłaBurgot, Jean-Louis. "Definitions of Acids and Bases: Strength of Acids and Bases". W Ionic Equilibria in Analytical Chemistry, 51–75. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-8382-4_4.
Pełny tekst źródłaZhang, Dequan, Xin Li, Li Chen, Chengli Hou i Zhenyu Wang. "Effects of Ionic Strength on Protein Phosphorylation". W Protein Phosphorylation and Meat Quality, 237–69. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-9441-0_11.
Pełny tekst źródłaChoppin, Gregory R. "Near Field and Far Field Interactions and Data Needs For Geologic Disposal of Nuclear Waste". W Actinide Speciation in High Ionic Strength Media, 3–10. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4419-8690-0_1.
Pełny tekst źródłaKarraker, D. G. "Plutonium (VI) Solubility Studies in Savannah River Site High-Level Waste". W Actinide Speciation in High Ionic Strength Media, 171–76. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4419-8690-0_10.
Pełny tekst źródłaBronikowski, M., O. S. Pokrovsky, M. Borkowski i G. R. Choppin. "UO2 2+ and NpO2 + Complexation with Citrate in Brine Solutions". W Actinide Speciation in High Ionic Strength Media, 177–85. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4419-8690-0_11.
Pełny tekst źródłaChen, Jian-Feng, Gregory R. Choppin i Robert C. Moore. "Complexation and Ion Interactions in Am(III)/EDTA/NaCl Ternary System". W Actinide Speciation in High Ionic Strength Media, 187–97. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4419-8690-0_12.
Pełny tekst źródłaLabonne-Wall, N., G. R. Choppin, C. Lopez i J.-M. Monsallier. "Interaction of Uranyl with Humic and Fulvic Acids at High Ionic Strength". W Actinide Speciation in High Ionic Strength Media, 199–211. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4419-8690-0_13.
Pełny tekst źródłaAguilar, Richard, Hans W. Papenguth i Fred Rigby. "Retardation of Colloidal Actinides Through Filtration in Intrusion Borehole Backfill at the Waste Isolation Pilot Plant (WIPP)". W Actinide Speciation in High Ionic Strength Media, 215–25. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4419-8690-0_14.
Pełny tekst źródłaStreszczenia konferencji na temat "Ionic strength"
Joshi, Punarvasu, Trupthi Mathew, Leo Petrossian, Shalini Prasad, Michael Goryll, Andreas Spanias i Trevor J. Thornton. "Electromigration of Charged Polystyrene Beads Through Silicon Nanopores Filled With Low Ionic Strength Solutions". W ASME 2009 International Mechanical Engineering Congress and Exposition. ASMEDC, 2009. http://dx.doi.org/10.1115/imece2009-11428.
Pełny tekst źródłaRomanovski, V. V. "Polymeric species of Pu in low ionic strength media". W Plutonium futures-The science (Topical conference on Plutonium and actinides). AIP, 2000. http://dx.doi.org/10.1063/1.1292289.
Pełny tekst źródłaOliveira, W. J., H. R. Soares, N. M. L. Silva, E. R. Souza i E. F. F. Silva. "Estimate of Ionic Strength of Solution for Each Electrical Conductivity". W II Inovagri International Meeting. Fortaleza, Ceará, Brasil: INOVAGRI/INCT-EI/INCTSal, 2014. http://dx.doi.org/10.12702/ii.inovagri.2014-a130.
Pełny tekst źródłaSEMPIONATTO, J. R., G. G. PEREZ, C. R. BASSO, I. CESARINO, S. A. S. MACHADO i V. A. PEDROSA. "SMART POLYMER MODIFIED ELECTRODE SWITCHED BY IONIC STRENGTH AND pH". W XX Congresso Brasileiro de Engenharia Química. São Paulo: Editora Edgard Blücher, 2015. http://dx.doi.org/10.5151/chemeng-cobeq2014-1202-20498-171803.
Pełny tekst źródłaRondinella, Vincenzo V., i M. John Matthewson. "Ionic effects on silica optical fiber strength and models for fatigue". W San Jose - DL tentative, redaktorzy Roger A. Greenwell i Dilip K. Paul. SPIE, 1991. http://dx.doi.org/10.1117/12.24684.
Pełny tekst źródłaYugami, Hiroo, Fumitada Iguchi, Kazuhisa Sato i Toshiyuki Hashida. "Mechanical Properties of Ceria Based Oxygen Ionic Conductors for SOFC". W ASME 2008 6th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2008. http://dx.doi.org/10.1115/fuelcell2008-65206.
Pełny tekst źródłaXiong, Yongliang, Yifeng Wang i Pholopoter Faltas. "Thermodynamic Model for Borate in Elevated Temperature and High Ionic Strength Environments". W Goldschmidt2020. Geochemical Society, 2020. http://dx.doi.org/10.46427/gold2020.2934.
Pełny tekst źródłaHalder, Bijoy K., i Angelica M. Palomino. "The Shear Strength of “Tunable” Clay-Polymer Composite under Various Ionic Concentrations". W Geo-Chicago 2016. Reston, VA: American Society of Civil Engineers, 2016. http://dx.doi.org/10.1061/9780784480151.007.
Pełny tekst źródłaSuzuki, T., Y. Morimoto, T. Hibino i S. Nakashita. "Influence of Adsorbed Ions and Ionic Strength in Sediment on Liquid Limit". W The 9th International Conference on Asia and Pacific Coasts 2017 (APAC 2017). WORLD SCIENTIFIC, 2017. http://dx.doi.org/10.1142/9789813233812_0037.
Pełny tekst źródłaPritam, Anil Arya i A. L. Sharma. "Improved ionic conductivity, potential window and dielectric strength in intercalated polymer nanocomposites". W DAE SOLID STATE PHYSICS SYMPOSIUM 2018. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5113424.
Pełny tekst źródłaRaporty organizacyjne na temat "Ionic strength"
Xu, Tianfu. TOUGHREACT Testing in High Ionic Strength Brine Sandstone Systems. Office of Scientific and Technical Information (OSTI), wrzesień 2008. http://dx.doi.org/10.2172/941168.
Pełny tekst źródłaNorton, John D., Wendy E. Benson, Henry S. White, Bradford D. Pendley i Hector D. Abruna. Voltammetric Measurement of Bimolecular Electron-Transfer Rates in Low Ionic Strength Solutions. Fort Belvoir, VA: Defense Technical Information Center, listopad 1990. http://dx.doi.org/10.21236/ada229913.
Pełny tekst źródłaPople, John A. The structure of pH dependent block copolymer micelles: charge and ionic strength dependence. Office of Scientific and Technical Information (OSTI), sierpień 2002. http://dx.doi.org/10.2172/799988.
Pełny tekst źródłaNorton, John D., i Henry S. White. Effect of Comproportionation on the Voltammetric Reduction of Methyl Viologen in Low Ionic Strength Solutions. Fort Belvoir, VA: Defense Technical Information Center, listopad 1991. http://dx.doi.org/10.21236/ada242444.
Pełny tekst źródłaNash, Charles A., L. Larry Hamm, Frank G. Smith i Daniel J. McCabe. Ion Exchange Distribution Coefficient Tests and Computer Modeling at High Ionic Strength Supporting Technetium Removal Resin Maturation. Office of Scientific and Technical Information (OSTI), grudzień 2014. http://dx.doi.org/10.2172/1166936.
Pełny tekst źródłaPhillips, S. L., C. A. Phillips i J. Skeen. Hydrolysis, formation and ionization constants at 25/sup 0/C, and at high temperature-high ionic strength. Office of Scientific and Technical Information (OSTI), luty 1985. http://dx.doi.org/10.2172/5911914.
Pełny tekst źródłaPhillips, S. Calculation of thermodynamic properties for monomeric U(IV) hydrolysis products at 298. 15 K and zero ionic strength. Office of Scientific and Technical Information (OSTI), styczeń 1990. http://dx.doi.org/10.2172/7159143.
Pełny tekst źródłaPendley, Bradford D., Hector D. Abruna, John D. Norton, Wendy E. Benson i Henry S. White. Analysis of Voltammetric Half-Wave Potentials in Low Ionic Strength Solutions and Voltammetric Measurement of Ion Impurity Concentrations. Fort Belvoir, VA: Defense Technical Information Center, listopad 1990. http://dx.doi.org/10.21236/ada229774.
Pełny tekst źródłaPendley, Bradford D., Hector D. Abruna, John D. Norton, Wendy E. Benson i Henry S. White. Analysis of Voltammetric Half-Wave Potentials in Low Ionic Strength Solutions and Voltammetric Measurement of Ion Impurity Concentrations. Fort Belvoir, VA: Defense Technical Information Center, listopad 1990. http://dx.doi.org/10.21236/ada229908.
Pełny tekst źródłaSwanson, Juliet. Effects of Salt Concentration, Ionic Strength, and Water Activity on the Growth of a WIPP Archaeal Isolate, Halobacterium sp. Office of Scientific and Technical Information (OSTI), listopad 2022. http://dx.doi.org/10.2172/1900474.
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