Showa Denko Shodex IC SI-50 4E User manual

Operation Manual Shodex IC SI-50 4E Version 211004E
Operation Manual
Shodex™ IC SI-50 4E
Europe, Middle East, Africa, Russia
www.shodex.de
Sales Office:
Showa Denko Europe GmbH
Shodex Business
Konrad-Zuse-Platz 3
81829 Munich
Germany
Technical Support:
[email protected]
+49 (0)89 / 93 99 62 37
Quotes and Orders:
[email protected]
+49 (0)89 / 93 99 62 34

Operation Manual Shodex IC SI-50 4E Version 211004E
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Operation Manual
Shodex IC SI-50 4E
(Please read this manual carefully to achieve the best and consistent column performance for a long time)
Important Handling Instructions
Caution! • Please consult the Safety Data Sheet (SDS) of reagents and solvents used with the
column and understand their proper handling methods to prevent potential health
hazards or death from occurring.
• Please wear appropriate personal protective equipment such as lab goggles and
gloves when handling organic solvents and acid and alkaline reagents. Avoid any direct
physical contact to prevent chemical injuries.
Before Using the Column
(1) Please visually inspect the package and outside of the column for any damage.
(2) Please check if product name and serial number written on the column package, column name tag,
and enclosed Certificate of Analysis (CoA) are matching and correct.
1. Introduction
Thank you for purchasing the Shodex™product. Shodex™IC SI-50 4E is a suppressor type ion
chromatography column for analysis of anions, using sodium carbonate eluents. The column is suitable
for the high performance analysis of standard inorganic anions including fluoride, chloride, nitrite,
bromide, nitrate, phosphate, and sulfate, as well as organic acid anions such as acetate and formic
acid.
2. Column Components
3. Column Specifications
Product Code
Product Name
Column Size ID x Length
Particle Size
Theoretical Plate
Number (Per Column)
F6995245
IC SI-50 4E
4.0 x 250 mm
5 µm
≥10,000
F6709625
IC SI-50G
4.6 x 10 mm
5 µm
(Guard Column)
Base Material: Spherical porous particles of polyvinyl alcohol modified with quaternary
ammonium group
Column Housing: PEEK
Screw type: Internally-threaded type No. 10-32 UNF
Shipping solvent: 3.2 mM Sodium Carbonate (Na2CO3) Solution + 1.0 mM Sodium Bicarbonate
(NaHCO3) Solution
Recommended storage:Fridge 4-8°C

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4. Usable Conditions
Product
Name
Flow Rate (mL/min)
Maximum
Pressure (MPa)
(Per Column)
pH
Range
Temperature (°C)
Recommended
Maximum
Recommended
Range
IC SI-50 4E
0.7
0.8
15
3 - 12
25
20 - 60
IC SI-50G
-
-
-
3 - 12
25
20 - 60
Usable solvents are listed below.
(1) In general, a mixture of sodium carbonate (Na2CO3) solution and sodium bicarbonate (NaHCO3)
solution is used.
(2) The standard eluent is 3.2 mM sodium carbonate solution and 1.0 mM sodium bicarbonate
solution. The higher the concentration of sodium carbonate solution, the faster the elution of ions will
be.
(3) Up to 10 % (v/v) acetonitrile or methanol is usable.
Attention! • Use the column within above stated flow rate, pressure, and temperature ranges.
Using the column outside the given range may damage the column and lower its
performance.
• Column pressure is influenced by the eluent composition, flow rate, and column
temperature. When changing the eluent compositions, adjust the flow rate and
column temperature so that the column pressure remains below the usable maximum
pressure.
5. Eluent Preparation
(1) Degas the eluent fully to prevent the formation of air bubbles.
(2) Presence of small debris or insoluble substances may result in deterioration of the column and/or
they appear as noise on the chromatograms. Filter the eluent with a 0.45 μm disposable filter to
prevent the problems.
Attention! • Whenever water is required, use ultra-pure water freshly generated by a water
purification system or water from a newly opened HPLC grade distilled water bottle.
Use HPLC grade organic solvent whenever possible. Solvents left in an opened bottle
for a long time should not be used. The content may have been changed, absorbed
moisture, or has been contaminated.
• Always use freshly prepared solvents. Solvents stored for a long time may have
changed their compositions and may influence elution patterns and/or damage the
column.
Note • Use of on-line degasser is recommended.
6. Sample Preparation
(1) Filter the sample solution using disposable 0.45 μm filter to prevent the column from clogging or
deteriorating.
(2) Recommended sample injection volume is less than 50 μL per column.
(3) For the samples containing proteins, remove the proteins prior to the sample injection. The use of
an ultrafiltration membrane is recommended.
(4) For the samples containing hydrophobic impurities, remove the impurities prior to the sample
injection. The use of a solid phase extraction is recommended.
Note •Use of guard column is recommended to protect the analytical column.

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7. Column Usage Procedure
7.1. HPLC System Preparation
Wash entire LC system prior to the column installation, including all flow-lines and sample loop by
switching the valve, and then replace the washing solution with the eluent to be used. If desired new
eluent has low miscibility/solubility to the eluent of previous analysis, first use the eluent that is
miscible/soluble to both eluents, and then replace it with the desired eluent.
Attention! • If the eluent left in the system is not compatible with the column to be used, it may
damage the column.
• A drastic change in the eluent compositions may remove substances adsorbed on
the system and they may enter and deteriorate the column.
7.2. Column Installation
(1) Connect the column to LC system by following the “flow direction arrow” () indicated on the
name tag. If guard column is used, position the guard column in front (before the inlet) of the analytical
column.
(2) Make sure to insert the tubing all the way to the end fitting and secure it with the male nut. It is
important that there is no extra space between the tubing and the column side of the end fitting.
Presence of an extra space will let the sample to spread out and may result in wide peaks.
(3) Set the initial flow rate at less than 0.3 mL/min and start the system. If using the column at an
elevated temperature, keep a low flow rate until the temperature of the column reaches to the set
temperature, and then gradually increase the flow rate to the desired.
Caution! • Verify that there is no solvent leak. It may cause electronic leakage, rust, and/or
chemical injury.
Attention! • Make sure not to let air bubbles enter the column while installing the column. The
air bubbles may damage the column.
• When restarting the system after column installation or after holding the eluent
flow, start the system at less than 0.3 mL/min. A rapid increase in pressure can damage
the column.
• If the column was used at an elevated temperature, lower the flow rate to less than
0.3 mL/min at the end of analysis. Then, turn off the column oven, and let the column
temperature return to room temperature before stopping the pump. If the pump was
stopped while the eluent inside the column was still hot, as the eluent temperature
decreases, its volume also decreases. This may result in creating an empty space in the
column and deteriorates the column.
Note •It is recommended to set the pump limiter to avoid exceeding the maximum
pressure.

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7.3. Solvent Exchange
When replacing the solvent, start the system at less than 0.3 mL/min. Recommended solvent volume
to introduce at each step is 3 to 5 times of the column volume.
7.4. Column Cleaning
Problems in peak shapes and elution time changes or elevated column pressure etc. are often caused
by insoluble or adsorbing components present in the eluent and reagents being deposited inside the
column. These problems may be resolved by cleaning the column.
If a guard column is used with the analytical column, first remove the guard column and check the
performance of the analytical column alone. If the problem is solved, most likely the cause is from the
guard column. In this case, clean the guard column.
If the problem is not solved by removing the guard column, clean both guard and analytical columns.
Make sure to clean the guard and the analytical columns separately. When washing the column, let
the washing solution flow from the column outlet go directly into the waste container and not let the
solution go through the detector.
<Cleaning Method>
(1) Insoluble components that block the column inlet may be removed by reversing the flow direction,
i.e., introducing the eluent from the column outlet, with flow rate at less than half of the recommended
flow rate.
(2) Follow below cleaning steps for adsorbing components. For an efficient cleaning, reverse the flow
direction and use the flow rate at 0.3 mL/min.
Method 1: Adsorption of hydrophilic compounds
Washing Solution
Cleaning Time
1
H2O
25 min
2
10 x Concentrated Eluent
100 min
3
H2O
25 min
4
Eluent (Return the column flow to normal direction)
100 min
Method 2: Adsorption of hydrophobic compounds
Washing Solution
Cleaning Time
1
H2O
25 min
2
H2O/CH3CN = 95/5
20 min
3
CH3CN
100 min
4
H2O
50 min
5
Eluent (Return the column flow to normal direction)
100 min
Attention! • Leaving the washing solution in the column for an extended time can damage the
column. Do not suspend the column cleaning but complete all procedures until the
last step to replace it with the eluent.