Скачать книгу

highly desired property in the ESTs, as it allows the pH to be stabilized with minimal increase in the conductivity.

      The total conductivity of the buffer must be higher than or close to the conductivity of the sample, otherwise it causes band destacking (Section 2.14). On the other hand, the lower the conductivity of the buffering electrolyte to the total conductivity of the buffer solution the better, as some room is left for the addition of some electrolytes with the same mobility as the analytes. This is important for the production of symmetric peaks in most of the separation modes. Isotachophoresis and isoelectric focusing are exceptions to this rule as they are based on special separation mechanisms. Some samples do have low conductivities, in this case the development of buffer solutions with low conductivity, i.e. designed for high field strengths operations, is always an active topic of research, [12] as they lead to high separation efficiencies (Section 3.5).

Grid chart depicting the buffer capacity of 0.1 M glycyl-aspartic acid (pKa = 2.81, 4.45 and 8.6) in an aqueous solution. Note the high buffer capacity at pH(I) = 3.6.
, 4.45 and 8.6) in an aqueous solution. Note the high buffer capacity at images.

      Another very useful concept is the normalized buffering capacity/conductivity ratio.[13] Here, the buffering capacity at each pH is divided by the buffer conductivity at this pH. A high buffer capacity and low buffer conductivity are highly desirable. This allows different buffers to be compared among themselves at different pHs. Such performance rankings of good buffers are still missing in the literature.

      Finally, there are a few applications (for instance the separation of aminium ions, quaternary ammonium ions, and coordination complexes) that can be run with pure propylene carbonate, formamide or other solvents, since the analytes remain charged within them. Moreover, propylene carbonate, for instance, does not produce gases at the electrodes, allowing the separation to be run in sealed systems.

      1 1 Reif, F. (1965). Fundamentals of Statistical and Thermal Physics. Tokyo: McGraw-Hill Kogakusha.

      2 2 Rahm, M., Zeng, T., and Hoffmann, R. (2019). Journal of the American Chemical Society 141: 342–351.

      3 3 Wohlfart, C. and Lechner, M.D. (eds.) (2008). Static Dielectric Constants of Pure Liquids and Binary Liquid Mixtures, Landolt–Börnstein. Berlin: Springer-Verlag.

      4 4 Soustelle, M. (2016). Ionic and Electrochemical Equilibria. Hoboken, NJ: Wiley.

      5 5 Franks, F. (1979). Water: A Comprehensive Treatise: Recent Advances, vol. 6. Boston, MA: Springer-Verlag.

      6 6 Connors, K.A. (2002). Thermodynamics of Pharmaceutical Systems. New York: Wiley.

      7 7 IUPAC (2012). Compendium of Chemical Terminology, Gold Book, Version 2.3.2. International Union of Pure and Applied Chemistry.

      8 8 Pitzer, K.S. (ed.) (1991). Activity Coefficients in Electrolyte Solutions, 2e. Boca Raton, FL: CRC Press.

      9 9 Reijenga, J.C., Gagliardi, L.G., and Kenndler, E. (2007). Journal of Chromatography A 1155: 142–145.

      10 10 Reijenga, J.C. (2009). Journal of Chromatography A 1216: 3642–3645.

      11 11 Gagliardi, L.G., Tascon, M., and Castells, C.B. (2015). Analytica Chimica Acta 889: 35–37.

      12 12 Hjertén, S., Valtcheva, L., Elenbring, K., and Liao, J.L. (1995). Electrophoresis 16: 584–594.

      13 13 Stoyanov, A.V. and Righetti, P.G. (1998). Electrophoresis. 19: 1674–1676.

      14 14 Schwer, C. and Kenndler, E. (1991). Analytical Chemistry 63: 1801–1807.

      15 15 Sarmini, K. and Kenndler, E. (1997). Journal of Chromatography A 792: 3–11.

      16 16 Sarmini, K. and Kenndler, E. (1998). Journal of Chromatography A 606: 325–335.

      17 17 Sarmini, K. and Kenndler, E. (1998). Journal of Chromatography A 811: 201–209.

      18 18 Sarmini, K. and Kenndler, E. (1998). Journal of Chromatography A 818: 209–215.

      19 19 Sarmini, K. and Kenndler, E. (1999). Journal of Chromatography A 833: 245–259.

      Конец ознакомительного фрагмента.

      Текст предоставлен ООО «ЛитРес».

      Прочитайте эту книгу целиком, купив полную легальную версию на ЛитРес.

      Безопасно оплатить книгу можно банковской картой Visa, MasterCard, Maestro, со счета мобильного телефона, с платежного терминала, в салоне МТС или Связной, через PayPal, WebMoney, Яндекс.Деньги, QIWI Кошелек, бонусными картами или другим удобным Вам способом.

/9j/4AAQSkZJRgABAQEBLAEsAAD/7R0gUGhvdG9zaG9wIDMuMAA4QklNBAQAAAAAACscAgAAAgAA HAJQAAlud2VocmthbXAcAgUAETk3ODExMTk1Mzk0MDcucGRmADhCSU0EJQAAAAAAEOEbZ3LY99no z3cuYnTtMlc4QklNBDoAAAAAAOUAAAAQAAAAAQAAAAAAC3ByaW50T3V0cHV0AAAABQAAAABQc3RT Ym9vbAEAAAAASW50ZWVudW0AAAAASW50ZQAAAABDbHJtAAAAD3ByaW50U2l4dGVlbkJpdGJvb2wA AAAAC3ByaW50ZXJOYW1lVEVYVAAAAAEAAAAAAA9wcmludFByb29mU2V0dXBPYmpjAAAADABQAHIA bwBvAGYAIABTAGUAdAB1AHAAAAAAAApwcm9vZlNldHVwAAAAAQAAA

Скачать книгу