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Analytical chemistry buffer solution

Over the last several years, the number of studies on application of artificial neural network for solving modeling problems in analytical chemistry and especially in optical fibre chemical sensor technology, has increase substantially69. The constructed sensors (e.g. the optical fibre pH sensor based on bromophenol blue immobilized in silica sol-gel film) are evaluated with respect to prediction of error of the artificial neural network, reproducibility, repeatability, photostability, response time and effect of ionic strength of the buffer solution on the sensor response. [Pg.368]

Potassium hydrogen phthalate has many uses in analytical chemistry. It is a primary standard for standardization of bases in aqueous solutions. Its equivalent weight is 204.2. It also is a primary standard for acids in anhydrous acetic acid. Other applications are as a buffer in pH determinations and as a reference standard for chemical oxygen demand (COD). The theoretical COD of a Img/L potassium hydrogen phthalate is 1.176mg O2. [Pg.757]

Sodium acetate is a mordant in dyeing. Other applications are in photography, as an additive to food, in purification of glucose, in preservation of meat, in tanning, and as a dehydrating agent. In analytical chemistry it is used to prepare buffer solution. [Pg.852]

Figure 33. Principle of proton-driven uphill transport for dopamine under a countertransport mode. The concentration of the carrier lasalocid A in o-dichlorobenzene was 0.1 M. The feed phase (100 ml) was 10 mM Tris-HCI buffer solution (pH 7.4) containing 1 mM ascorbic acid. The receiving phase (0.5-2.0 ml) was a hydrochloric acid solution (pH 0.5-3.0). The initial dopamine concentration in the feed solution was in the range from 1.00 x 10 to 1.00 x 10 M (reprinted with permission from Anal. Sci. 1996, 12, 333. Copyright 1996 The Japan Society for Analytical Chemistry). Figure 33. Principle of proton-driven uphill transport for dopamine under a countertransport mode. The concentration of the carrier lasalocid A in o-dichlorobenzene was 0.1 M. The feed phase (100 ml) was 10 mM Tris-HCI buffer solution (pH 7.4) containing 1 mM ascorbic acid. The receiving phase (0.5-2.0 ml) was a hydrochloric acid solution (pH 0.5-3.0). The initial dopamine concentration in the feed solution was in the range from 1.00 x 10 to 1.00 x 10 M (reprinted with permission from Anal. Sci. 1996, 12, 333. Copyright 1996 The Japan Society for Analytical Chemistry).
Fig. 14.45. Amperometric recordings from a single canine pancreatic (3-cell bathed in Ca2+-free physiological buffer. Bars indicate the application of solution from a micropipette. In the trace on the left, the solution applied was Ca2+-free physiological buffer with 64 mM K+. (Reprinted from Lan Huang and Robert Kennedy, Exploring Single-Cell Dynamics Using Chemically-Modified Microelectrodes, in Trends in Analytical Chemistry, Vol. 14, p. 160, Fig. 3, copyright 1995, with permission from Elsevier Science.)... Fig. 14.45. Amperometric recordings from a single canine pancreatic (3-cell bathed in Ca2+-free physiological buffer. Bars indicate the application of solution from a micropipette. In the trace on the left, the solution applied was Ca2+-free physiological buffer with 64 mM K+. (Reprinted from Lan Huang and Robert Kennedy, Exploring Single-Cell Dynamics Using Chemically-Modified Microelectrodes, in Trends in Analytical Chemistry, Vol. 14, p. 160, Fig. 3, copyright 1995, with permission from Elsevier Science.)...
Control of pH is vital in synthetic and analytical chemistry, just as it is in living organisms. Procedures that work well at a pH of 5 may fail when the concentration of hydronium ion in the solution is raised tenfold to make the pH 4. Fortunately, it is possible to prepare buffer solutions that maintain the pH close to any desired value by the proper choice of a weak acid and the ratio of its concentration to that of its conjugate base. Let s see how to choose the best conjugate acid-base system and how to calculate the required acid-base ratio. [Pg.647]

Textbooks of analytical chemistry should be consulted for further details concerning the ionization of weak acids and bases and the theory of indicators, buffer solutions, and acid-alkali titrations. [Pg.48]

Figure 3 Separation of a standard solution of d- and L-amino acids by chiral derivatization with ( + )-1-(9-fluorenyl)ethyl chioroformate foiiowed by high-performance liquid chromatography on an achiral column. Column Spherisorb octyl material (150 X 4.6 mm). Mobile phase acetonitrile (ACN), tetrahydrofuran (THF), and an acetic acid buffer (1.8 ml of glacial acetic acid in 11 of water pH adjusted to 4.35 with NaOH) Gradient 0-8 min, 8% ACN, 17% THF, 75% buffer (8/17/75) 8-22 min, 8/17/75 to 0/30/70 22-70 min, 0/30/70 to 0/50/50. Flow rate 0.8 ml min (Reprinted with permission from Einarsson S, Josefsson B, Moller P, and Sanchez D (1987) Analytical Chemistry 59 1194 American Chemical Society.)... Figure 3 Separation of a standard solution of d- and L-amino acids by chiral derivatization with ( + )-1-(9-fluorenyl)ethyl chioroformate foiiowed by high-performance liquid chromatography on an achiral column. Column Spherisorb octyl material (150 X 4.6 mm). Mobile phase acetonitrile (ACN), tetrahydrofuran (THF), and an acetic acid buffer (1.8 ml of glacial acetic acid in 11 of water pH adjusted to 4.35 with NaOH) Gradient 0-8 min, 8% ACN, 17% THF, 75% buffer (8/17/75) 8-22 min, 8/17/75 to 0/30/70 22-70 min, 0/30/70 to 0/50/50. Flow rate 0.8 ml min (Reprinted with permission from Einarsson S, Josefsson B, Moller P, and Sanchez D (1987) Analytical Chemistry 59 1194 American Chemical Society.)...
Figure 2 Polarograms of tetracycline in acetate buffer. (1) Conventional (d.c.) polarogram of a 150mg 1 solution. (2) Differential pulse polarogram of a 1 mg 1 solution. (Reprinted from Analytical Chemistry September 1972, 44(11) 75A-87A. Published 1972, American Chemical Society.)... Figure 2 Polarograms of tetracycline in acetate buffer. (1) Conventional (d.c.) polarogram of a 150mg 1 solution. (2) Differential pulse polarogram of a 1 mg 1 solution. (Reprinted from Analytical Chemistry September 1972, 44(11) 75A-87A. Published 1972, American Chemical Society.)...
Nanomaterials in the form of a colloidal solution or quantum dots are attributed to have a tremendous impact in analytical chemistry for their unique physical and chemical properties (Alivisatos 2004 Katz and Willner 2004). A different methodology has been adopted to analyse vitamin Bi spectro-fluorimetrically by using cadmium selenide quantum dots (CdSe QDs), cadmium telluride (CdTe) nanorods, and silica and gold nanoparticles. A fluorescence resonance Rayleigh scattering (RRS) method was applied for determining vitamin Bi at sub-nanomolar level (Liu et al. 2006). In this technique, vitamin Bi was mixed with acidic buffer and prepared gold nanoparticles. After incubation, the solution mixture was excited in synchronous mode to obtain RRS spectra. The RRS spectral intensity correlated with the concentration of vitamin Bi. [Pg.249]

Subarats X, Bosch E, Roses M (2007) Retention of ionizable compounds on high-performance liquid chromatography. XVll. Estimation of the pH variation of aqueous buffers with the change of the methanol fraction ofthe mobile phase. J Chromatogr A 1138 203-215 Siicha E, Kotrly S (1972) Solution Equilibria in Analytical Chemistry. Reinhold, London Butler JN, Cogley DR (1998) Ionic Equilibrium. Solubility and pH Calculations. Wiley, New York... [Pg.198]

In UHPLC, a generic gradient is generally used to cover the widest polarity range possible. To improve the MS sensitivity and limit the number of unwanted interactions between analytes and residual silanols on the surface of the stationary phase, 0.1% formic acid is added to the mobile phase. Only a few authors have reported the use of buffer solutions to control the pH to obtain a more robust selectivity. A C18 chemistry-based stationary phase of 50-100 mm is generally combined with... [Pg.113]

All solvents and chemicals were HPLC grade. Organic solvents, sodium carbonate (anhydrous), and sodium bicarbonate were purchased from Fisher Scientific (Fair Lawn, NJ, USA). Carbonate buffer, pH = 10.0, was prepared using the sodium carbonate (anhydrous), and sodium bicarbonate. A solution of 0.1 % triethylamine in methanol was made for the elution solvent. Diethylcarbamazine citrate was obtained from Sigma, and used to make stock solutions (St. Louis, MO, USA). The internal standard, 1-diethylcarbamyl-4-ethylpiperazine (E-DEC) was synthesized by the Division of Medicinal and Natural Products Chemistry at the University of Iowa, College of Pharmacy. Ultra-pure analytical grade Type I water was produced by a Milli-Q Plus water system (Millipore Corporation, Bedford, MA, USA). For the extraction of DEC and of its internal standard, Alltech Extract - Clean C18 cartridges, 500 mg with a 2.8 mL reservoir, and a SPE vacuum manifold (Alltech, Deerfield, IL, USA) were used. [Pg.641]


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Analyte, solution

Analytes solution

Analytic solutions

Analytical chemistry analyte

Analytical chemistry analytes

Analytical solutions

Buffer solutions

Buffered solution

Chemistry analytical

Solute chemistry

Solution chemistry

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