Hamilton 79397 Ion Exclusion HPLC Column, PRP-X300 7 µm 2.1 x 250 mm
Ion exclusion chromatography is an alternative to ion exchange chromatography in which ionized samples are excluded from the pores of the support and elute first, while the weakly ionized and nonionic compounds elute later. Mixtures of weak acids, like those in fruits and milk products, are frequently not very well separated by pure ion-exchange methods, nor in the reversed-phase mode.
Specifications
Stationary Phase | PRP-X300 |
Mode | Ion Exclusion |
USP Classification | USP L22 |
Packing Material Type | PSDVB/Sulfonic Acid |
Particle Size | 7 µm |
Pore Size | 100 Å |
Format | Column |
Hardware Inner Diameter | 2.1 mm |
Hardware Length | 250 mm |
Hardware Material | Stainless Steel |
Max. Pressure | 5,000 psi |
Max. Pressure | 5000 |
Exchange Capacity | 0.17 meq/gm |
Mobile Phase Limits | pH 1-13. 0-100% aqueous, organic modifier |
Buffer Strength | 0.0-0.5N |
Temp Limits | 5-60°C |
Restoration | Inject several times with 100 µL of 1 N nitric acid |
Compound Classification | Organic Acids/Alcohols |
Hamilton PRP-X300 columns offer an easy, rapid way to separate closely related alcohols and organic acids. The sulfonated poly(styrene-divinylbenzene) support separates samples via a mixed mode mechanism. Separation on the PRP-X300 is accomplished by three modes:
- Hydrogen Bonding—The attraction and retention of sample compounds by the negatively charged sulfonate group.
- Reversed-Phase—The interaction and retention of the sample compounds by the non-polar polymeric support.
- Ion Exclusion—The process in which ionized samples are excluded from the pores of the support and elute first, while the weakly ionized and nonionic compounds elute later.
Reversed Phase Columns
Packing Name | Support Material | Exchange Capacity | Pore Size | Temp. Limits | Mobile Phase Limits | Buffer Strength | Maximum Pressure |
PRP-1 | PSDVB* | N/A | 100 Å | 5-85 °C | pH 1-13. 0-100% aqueous, organic modifier | 0.0-0.5N | 5,000 psi |
PRP-C18 | C18 bonded to PSDVB* | N/A | 100 Å | 5-85 °C | pH 1 – 13. 0-100% aqueous, organic modifier | 0.0-0.5N | 5,000 psi |
PRP-3 | PSDVB* | N/A | 300 Å | 5-85 °C | pH 1-13. 0-100% aqueous, organic modifier | 0.0-0.5N | 5,000 psi |
PRP-h5 | Fluorinated PSDVB* | N/A | 300 Å | 5-85 °C | pH 1 – 13. 0-100% aqueous, organic modifier | 0.0-0.5N | 5,000 psi |
HxSil C18 | Silica | N/A | 110 Å | 5-60 °C | pH 1.5 – 10. 0-100% aqueous, organic modifier | N/A | 6,000 psi |
HxSil C8 | Silica | N/A | 110 Å | 5-60 °C | pH 1.5 – 10. 0-100% aqueous, organic modifier | N/A | 6,000 psi |
Anion Exchange Columns
Packing Name | Support Material | Exchange Capacity | Pore Size | Temp. Limits | Mobile Phase Limits | Buffer Strength | Maximum Pressure |
PRP-X100 | PSDVB* with Tri- methyl ammonium Exchanger | 0.19meq/gm | 100 Å | pH Dependent** | pH 1-13. 0-100% aqueous, organic modifier | 0.0-0.5N | 5,000 psi |
PRP-X110 | PSDVB* with Tri-methyl ammonium Exchanger | 0.11meq/gm | 100 Å | pH Dependent** | pH 1-13. 0-100% aqueous, organic modifier | 0.0-0.5N | 5,000 psi |
PRP-X500 | Poly(meth-acryl amido-propyl Trimethyl-ammonium chloride) | 1.6meq/gm | Superficially porous | pH Dependent** | pH 1-13. 0-100% aqueous, organic modifier | 0.0-2.0N | 5,000 psi |
PRP-X600 | Poly (di-methyl amido-propyl meth-acrylamide) | 1.6meq/gm | Superficially porous | pH Dependent** | pH 1-13. 0-100% aqueous, organic modifier | 0.0-1.0N | 5,000 psi |
RCX-10 | PSDVB* with Tri-methyl ammonium Exchanger | 0.35meq/gm | 100 Å | pH Dependent** | pH 1-13. 0-100% aqueous, organic modifier | 0.0-1.0N | 5,000 psi |
RCX-30 | PSDVB* with Tri-methyl ammonium Exchanger | 1.0meq/gm | 100 Å | pH Dependent** | pH 1-13. 0-100% aqueous, organic modifier | 0.0-1.0N | 5,000 psi |
Cation Exchange Columns
Packing Name | Support Material | Exchange Capacity | Pore Size | Temp. Limits | Mobile Phase Limits | Buffer Strength | Maximum Pressure |
PRP-X200 | PSDVB* Sulfonate Exchanger | 35ueq/gm | 100 Å | 5-60 °C | pH 1-13. 0-100% aqueous, organic modifier | 0.0-0.5N | 5,000 psi |
PRP-X400 | PSDVB* Sulfonate Exchanger | 2.5meq/gm | N/A | 5-60 °C | pH 1-13. 0-100% aqueous, organic modifier | 0.0-5.0N | 5,000 psi |
PRP-X800 | PSDVB* Itaconate Exchanger | 1.6meq/gm | 100 Å | 5-60 °C | pH 1-13. 0-100% aqueous, organic modifier | 0.0-0.5N | 5,000 psi |
HC-40 Calcium | PSDVB* Sulfonate Exchanger | 5meq/gm | Gel-type | 25-90 °C | 100% Water | Water | 1,000 psi |
HC-75 Calcium | PSDVB* Sulfonate Exchanger | 5meq/gm | Gel-type | 25-90 °C | 100% Water 0-40% Acetonitrile | Water | 400 psi |
HC-75 Hydrogen | PSDVB* Sulfonate Exchanger | 5meq/gm | Gel-type | 25-90 °C | 100% Water 0-40% Acetonitrile | Water | 400 psi |
HC-75 Lead | PSDVB* Sulfonate Exchanger | 5meq/gm | Gel-type | 25-90 °C | 100% Water 0-40% Acetonitrile | Water | 400 psi |
Ion Exclusion Columns
Packing Name | Support Material | Exchange Capacity | Pore Size | Temp. Limits | Mobile Phase Limits | Buffer Strength | Maximum Pressure |
PRP-X300 | PSDVB* Sulfonate Exchanger | 0.17meq/gm | 100 Å | 5-60 °C | pH 1-13. 0-100% aqueous, organic modifier | 0.0-0.5N | 5,000 psi |
*PSDVB is Poly(styrene-divinylbenzene)
**pH 1-7.9 Temp. 5-60 °C; pH 8-13 Temp. 5-30 °C
An HPLC column has a finite lifetime. It is recommended that you routinely monitor a column's retention characteristic and performance using standards. If you plan to store the column for a prolonged period of time, use a mobile phase that inhibits microbial growth (a mobile phase containing sodium azide or high concentrations of methanol, acetonitrile, etc.). For optimum performance and column life, follow these recommendations.
- Routinely monitor the column's performance.
- Switch only between miscible mobile phases.
- Avoid precipitating salts in the column.
- Use filtered and degassed mobile phases.
- Do not allow the column to dry out. Keep it tightly capped when not in use.
- For prolonged storage, use a mobile phase that inhibits bacterial and mold growth.
- Use the column in the direction indicated on the label. An unusually high operating pressure may indicate a plugged inlet frit and may be cleared by reversing flow through the column for 10-20 mL.
- Use Hamilton guard columns to remove particulate matter or impurities that may permanently bind to the analytical column.
Restoring Column Performance
The procedures listed below may restore the performance of a column that has become fouled, but the procedures will not improve the performance of a column that is damaged or beyond its useful life. Nor can all stationary phases be restored. The unique supports in PRP-X500 and PRP-X600 columns make it impossible to restore performance with a washing procedure. For technical assistance regarding these columns, please Contact HPLC Support. NOTE: Before performing a restoration procedure, always make sure that the mobile phases are miscible and that precipitation will not occur. If necessary, wash the column with a suitable intermediate solvent before changing over to the new mobile phase. A minimum of five column volumes of intermediate solvent should be used.
Column Restoration Procedures
Follow the appropriate restoration procedure listed below using a flow rate of 1.0 or 2.0 mL/min. unless otherwise specified. Evaluate column performance using the test mix and conditions listed on the Performance Test Report shipped with each column.
Column Restoration Procedures
Packing Material Name
|
Restoration Procedure |
PRP-C18 |
Flush with 40:40:20 (ACN:IPA:H20) for 5-10 column volumes. |
PRP-1 | |
PRP-3 |
|
PRP-h5 |
|
HxSil C8 |
|
HxSil C18 |
|
PRP-X100 |
Pump approximately 50 mL of methanol with 1% 6 N nitric acid |
PRP-X200 |
Inject several times with 100 µL of 1 N nitric acid |
PRP-X300 |
|
PRP-X400 |
Inject Several times with 100 µL of 0.1 M potassium EDTA |
RCX-10 |
Flush with 50 mL 0.1 N sodium hydroxide |
RCX-30 |
Flush with 150 mL 0.1 N sodium hydroxide |
HC-40 |
Ca2+ Flush with 1% calcium chloride at 0.1 mL/min overnight |
HC-75 |
Ca2+ Flush with 1% calcium chloride at 0.1 mL/min overnight |
|
H+ Flush with 0.1 N sulfuric acid at 0.1 mL/min overnight |
|
Pb2+ Flush with 1% lead nitrate at 0.1 mL/min overnight |