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Buffer solution preparation

CI8-OOO2. Calculate the concentrations of the major species present in a buffer solution prepared by adding 1.40 g NaOH to 140. mL of 0.750 M NH4 Cl. [Pg.1276]

As a measure of their thermodynamic stability, the pAfR+ values for the carbocation salts were determined spectrophotometrically in a buffer solution prepared in aqueous solution of acetonitrile. The KR+ scale is defined by the equilibrium constant for the reaction of a carbocation with water molecule (/CR+ = [R0H][H30+]/[R+]). Therefore, the larger p/CR+ index indicates higher stability for the carbocation. However, the neutralization of these cations was not completely reversible. This is attributable to instability of the neutralized products. The instability of the neutralized products should arise from production of unstable polyolefinic substructure by attack of the base at the aromatic core. [Pg.177]

It should be stressed that the pH value of an actual buffer solution prepared by mixing quantities of the weak acid or base and its conjugate base or acid based on the calculated ratio will likely be different from what was calculated. The reason for this is the use of approximations in the calculations. For example, the molar concentration expressions found in Equations (5.23) to (5.30), e.g., [H+], are approximations. To be thermodynamically correct, the activity of the chemical should be used rather than the concentration. Activity is directly proportional to concentration, the activity coefficient being the proportionality constant ... [Pg.116]

What is the pH value of a 1 L buffer solution prepared by mixing 0.1 M NH3 solution with 96.3 g NH4CI (assume no volume change) ... [Pg.131]

Substrate/buffer solution (prepare fresh) Mix 75 pi oleic acid, 50 pi taurocholate and 250 pi 6-hexadecanoylamino-4-methylumbelliferyl- /3-d-galactopyranosidc stock solution in a 1.5-ml Eppendorf vial and take the mixture to dryness under a gentle stream of nitrogen. Add 500 pi of reaction buffer at room temperature,... [Pg.364]

Buffer Solutions, Prepare buffer solns of the following pH s at 25° C by mixing the... [Pg.166]

PROBLEM 16.9 Use the Henderson-Hasselbalch equation to calculate the pH of a buffer solution prepared by mixing equal volumes of 0.20 M NaHC03 and 0.10 M Na2C03. (,Ka values are given in Appendix C.)... [Pg.678]

Electrolyte pH 4.5, 0.1M acetate buffer solution prepared using analytical grade reagents and purified water from a Millipore Milli-Q system (conductivity < 0.1 iS/cm). DNA solutions obtained by direct dilution of the appropriate volume in acetate buffer. [Pg.1152]

The chromatographic procedure may be carried out using (a) two stainless steel columns in series the first (25 cm x 4.6 mm) packed with particles of silica, the surface of which has been modified with chemically bonded hexysilyl groups (5 /im) (Spherisorb C6 is suitable) and the second (25 cm x 4.6 mm) packed with cation exchange resin (10 /an) (Partisil-10 SCX is suitable) (b) as the mobile phase at a flow rate of 1.0 ml/min, a mixture of 25 volumes of acetonitrile, 25 volumes of a phosphate buffer solution prepared by dissolving 58.5 g of sodium dihydrogen orthophosphate... [Pg.326]

The pH reference materials were selected also to cause small liquid junction potential < 0.01 in pH if the pH of the buffer solution prepared from this material is measured in cells with transference [12]. The molality of the primary buffer solutions are kept at < 0.1 mol kg-1 for the same reason [13]. Furthermore, the primary buffers have a long-time stability of stored solid material (>3 years), except solid borax buffer material. Borax buffer (0.1 mol kg-1) has a restricted stability of about 2 years only [14]. [Pg.209]

Consider the buffer solution prepared by mixing together acetic acid—... [Pg.175]

Magnesium-Chelating Substances Transfer 1 g of sample, accurately weighed, into a small beaker, and dissolve it in 5 mL of water. Add 5 mL of a buffer solution prepared by dissolving 67.5 g of ammonium chloride in 200 mL of water, adding 570 mL of ammonium hydroxide, and diluting with water to 1000 mL. Then add 5 drops of eriochrome black TS to the buffered solution, and titrate with 0.1 M magnesium acetate to the appearance of a deep wine red color. Not more than 2.0 mL is required. [Pg.66]

No-Indicator Buffer Solution Prepare a mixture consisting of 700 mL of 0.1 M citric acid (anhydrous, reagent grade), 200 mL of 0.2 M disodium phosphate, and 100 mL of spectrograde methanol. [Pg.115]

Sample Preparation Transfer 1 g of sample, accurately weighed, into a 400-mL beaker, and add 40 mL of Mixed 8.2 Buffer Solution. Prepare four samples (two sets of duplicates). Use the two sets to prepare digested samples for the Determination of Total Fiber and for the Determination of Soluble Fiber. [Pg.459]

Add 1 drop of methyl violet indicator solution and introduce dilute HC1 or dilute NH3 solution (as necessary) dropwise and with constant stirring until the colour of the solution is yellow-green a blue-green colour is almost but not quite acid enough, yet it is acceptable for most analyses. (If the indicator paper is available, the thoroughly stirred solution should be spotted on fresh portions of the paper.) It is recommended that a comparison solution containing, say, 10 ml of 0-3m HC1 and 1 drop of indicator be freshly prepared this will facilitate the correct adjustment of the acidity. A more satisfactory standard is a buffer solution prepared by mixing 5 ml of m sodium acetate, 5 ml of 2m HC1, and 5 ml of water this has a pH of 0-5. [Pg.562]

Number 8 16 x 150 mm test tubes and place them in a test tube rack. Into each tube carefully pipette 0.10 ml of the bromophenol blue solution. 2-67. Into each of the tubes carefully pipette 12.0 ml of one of the buffer solutions prepared in steps 2-62 and 2-64. [Pg.59]

Consider the buffer solution prepared by mixing together acetic acid—HC2H3O2—and sodium acetate—C2H3O2- containing Na+ as a spectator ion (See Skill 2.1b). The equilibrium reaction for this acid/conjugate base pair is ... [Pg.76]

The Buffer Process Addition of Base (OH ) to a Buffer Solution Addition of Acid (H3O+) to a Buffer Solution Preparation of a Buffer Solution... [Pg.235]

Calculate the pH of a buffer solution prepared by dissolving 21.5 g benzoic acid (HC7H5O2) and 37.7 g sodium benzoate In 200.0 mL of solution. [Pg.737]

C. Consider a buffer solution prepared by mixing 5.00 mmol of Na2C204 (sodium oxalate) with 2.50 mmol of HCl in 0.100 L. [Pg.268]

For water and heavy water, the values of the ionization constant at 25°C are 1.00 x 10 and 1.38 x 10 , which correspond to pH and pD values of 7.0 and 7.43, respectively. This has a practical consequence in the determination of pD values by glass electrodes (Glasoe and Long 1960) if the pH meter is calibrated by using buffer solutions prepared with H2O, then one must... [Pg.704]


See other pages where Buffer solution preparation is mentioned: [Pg.588]    [Pg.101]    [Pg.117]    [Pg.331]    [Pg.37]    [Pg.308]    [Pg.713]    [Pg.417]    [Pg.483]    [Pg.446]    [Pg.581]    [Pg.803]    [Pg.239]    [Pg.278]    [Pg.803]    [Pg.63]    [Pg.222]    [Pg.44]    [Pg.304]   
See also in sourсe #XX -- [ Pg.258 ]

See also in sourсe #XX -- [ Pg.625 ]

See also in sourсe #XX -- [ Pg.799 , Pg.800 , Pg.801 ]




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