Product Manual for IonPac CS16
Page 18 of 65
Therefore, for a 1 N H
2
SO
4
solution, weigh out:
1
liter
x 98.08
g
x 1
mole
x 1
mole
x 100
g
= 50.04
g
1 mole
2 Eq
liter
98 g
4.4.3.
Eluent Preparation
________ ________ ________ ________
Eluent: X mN Sulfuric Acid (H
2
SO
4
) or Methanesulfonic acid (MSA)
Using the table below, pipet x.0 mL of the 1.0 N H
2
SO
4
or 1.0 N MSA eluent concentrate (see Section 5.1, “Preparation of
Eluent Stock Solution Concentrates”) into a 1-L volumetric flask. Dilute to 1-L using deionized water with a specific
resistance of 18.2 megohm-cm. Degas the eluent.
Table 6
mN Eluents from Stock Solutions
mN
H
2
SO
4
or MSA
# mL
H
2
SO
4
or MSA
4 4.0
10 10.0
16 16.0
18 18.0
20 20.0
22 22.0
24 24.0
30 30.0
40 40.0
100 100.0
4.5.
Eluents with Solvents
Solvents can be added to the ionic eluents used with IonPac CS16 columns to modify the ion exchange process or improve
sample solubility. The solvents used must be free of ionic impurities. However, since most manufacturers of solvents do not
test for ionic impurities, it is important that the highest grade of solvents available be used. Currently, several manufacturers
are making ultrahigh purity solvents that are compatible for HPLC and spectrophotometric applications. These ultrahigh
purity solvents will usually ensure that your chromatography is not affected by ionic impurities in the solvent. Currently at
Dionex, we have obtained consistent results using High Purity Solvents manufactured by Burdick and Jackson and Optima
®
Solvents by Fisher Scientific.
When using a solvent in an ionic eluent, column back pressures will depend on the solvent used, concentration of the solvent,
the ionic strength of the eluent and the flow rate used. The column back pressure will vary as the composition of water-
acetonitrile mixture varies. The practical back pressure limit for the IonPac CS16 columns is 4,000 psi (27.57 MPa).
The IonPac CS16 is compatible with the HPLC solvents listed in Table 7, “HPLC Solvents for Use with the CS16 Columns.”
Alcohols, however, should be avoided, since the column capacity for cation exchange may be reduced due to the reversible
formation of esters in the column packing. Solvents and water should be premixed in concentrations which allow proper
mixing by the gradient pump and to minimize outgassing. Ensure that all of the inorganic chemicals are soluble in the highest
solvent concentration to be used during the analysis.
Document No. 031747-05
© 2010 Dionex Corporation
December 2010
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